Experiment 1. Nucleophilic aromatic substitution. Introduction

Similar documents
EXPERIMENT 3 (Organic Chemistry II) Nitration of Aromatic Compounds: Preparation of methyl-m-nitrobenzoate

experiment5 Understanding and applying the concept of limiting reagents. Learning how to perform a vacuum filtration.

Page 1 of 5. Purification of Cholesterol An Oxidative Addition-Reductive Elimination Sequence

4026 Synthesis of 2-chloro-2-methylpropane (tert-butyl chloride) from tert-butanol

Experiment 8 Synthesis of Aspirin

PURIFICATION TECHNIQUES

The Aldol Condensation

Synthesis of Aspirin and Oil of Wintergreen

Syllabus CHM 2202 Organic Chemistry Laboratory II Spring 2011

CHEM 2423 Recrystallization of Benzoic Acid EXPERIMENT 4 - Purification - Recrystallization of Benzoic acid

Online edition for students of organic chemistry lab courses at the University of Colorado, Boulder, Dept of Chem and Biochem.

H H H O. Pre-Lab Exercises Lab 6: Organic Chemistry. Lab 6: Organic Chemistry Chemistry Define the following: a.

Enantiomers: Synthesis, characterization, and resolution of tris(ethylenediamine)cobalt(iii) chloride Introduction:

Chapter 5 Classification of Organic Compounds by Solubility

ISOLATION OF CAFFEINE FROM TEA

AIRFREE TECHNIQUE AND SENSITIVE REAGENTS S ECTI O N 1: GLASS W ARE A ND E Q UIP M ENT. A. Using a manifold

Reminder: These notes are meant to supplement, not replace, the textbook and lab manual. Electrophilic Aromatic Substitution notes

Separation by Solvent Extraction

14 Friedel-Crafts Alkylation

Green Principles Atom Economy Solventless Reactions Catalysis

Isolation of Caffeine from Tea

PREPARATION AND PROPERTIES OF A SOAP

Experiment 3: Extraction: Separation of an Acidic, a Basic and a Neutral Substance

Synthesis of Isopentyl Acetate

Table 1. Common esters used for flavors and fragrances

REACTIONS OF AROMATIC COMPOUNDS

EXPERIMENT Aspirin: Synthesis and NMR Analysis

CH243: Lab 4 Synthesis of Artificial Flavorings by Fischer Esterification

Saturated NaCl solution rubber tubing (2) Glass adaptor (2) thermometer adaptor heating mantle

CHEM 322 Organic Chemistry II - Professor Kathleen V. Kilway. CHAPTER 14 Substitution Reactions of Aromatic Compounds

A Greener Synthesis of Creatine

Alkoxycarbonylation of Ethylene with Cellulose in Ionic Liquids

Determination of Molar Mass by Boiling Point Elevation of Urea Solution

Organic Chemistry Lab Experiment 4 Preparation and Properties of Soap

CHM220 Addition lab. Experiment: Reactions of alkanes, alkenes, and cycloalkenes*

In this experiment, we will use three properties to identify a liquid substance: solubility, density and boiling point..

CHEM 211 CHAPTER 16 - Homework

Physical and Chemical Properties and Changes

EXPERIMENT 2 (Organic Chemistry II) Pahlavan/Cherif Diels-Alder Reaction Preparation of ENDO-NORBORNENE-5, 6-CIS-CARBOXYLIC ANHYDRIDE

Properties of Acids and Bases

SYNTHESIS AND ANALYSIS OF A COORDINATION COMPOUND OF COPPER

Name Lab #3: Solubility of Organic Compounds Objectives: Introduction: soluble insoluble partially soluble miscible immiscible

Experiment 12- Classification of Matter Experiment

Experiment 14 Preparation of p-nitroaniline

Physical Properties of a Pure Substance, Water

The Properties of Water (Instruction Sheet)

oxidize 4-Cholesten-3-one

PHYSICAL SEPARATION TECHNIQUES. Introduction

Partner: Jack 17 November Determination of the Molar Mass of Volatile Liquids

CHM220 Nucleophilic Substitution Lab. Studying S N 1 and S N 2 Reactions: Nucloephilic Substitution at Saturated Carbon*

CHEM 322: Azo Dyes: Combinatorial Synthesis of Dyes

Hands-On Labs SM-1 Lab Manual

Benzene Benzene is best represented as a resonance hybrid:

Electrophilic Aromatic Substitution Reactions

The most common active ingredient used in deodorants is aluminium chlorohydrate. But not all deodorants contain aluminium chlorohydrate:

The Grignard Reaction. Preparation of Benzoic Acid

Chemistry Notes for class 12 Chapter 13 Amines

Electrophilic Aromatic Substitution

EXPERIMENT 1 (Organic Chemistry I)

Q.1 Draw out some suitable structures which fit the molecular formula C 6 H 6

Taking Apart the Pieces

Properties of Alcohols and Phenols Experiment #3

GRIGNARD REACTION: PREPARATION OF TRIPHENYLMETHANOL (12/22/2009)

Chemical versus Physical Changes

One problem often faced in qualitative analysis is to test for one ion in a

THIN LAYER CHROMATOGRAPHY AND MELTING POINT DETERMINATION: DETECTION OF CAFFEINE IN VARIOUS SAMPLES

PREPARATION FOR CHEMISTRY LAB: COMBUSTION

The Synthesis of trans-dichlorobis(ethylenediamine)cobalt(iii) Chloride

#10 Condensation Polymerization: Preparation of Nylon 6/6

and its application in the synthesis of Nilotinib intermediate

Mixtures and Pure Substances

Determination of Melting Points

Reactions of Aldehydes and Ketones

Laboratory 22: Properties of Alcohols

EXPERIMENT 9 (Organic Chemistry II) Pahlavan - Cherif Synthesis of Aspirin - Esterification

CHEMICAL REACTIONS OF COPPER AND PERCENT YIELD KEY

Solubility Curve of Sugar in Water

AN EXPERIMENT IN ALCHEMY: COPPER TO SILVER TO GOLD 2005, 2000, 1996 by David A. Katz. All rights reserved

Chapter Test A. Elements, Compounds, and Mixtures MULTIPLE CHOICE. chemically combined? MIXs2 a. element b. compound c. mixture d.

Organic Lab 1 Make-up Experiment. Extraction of Caffeine from Beverages. Introduction

Preparation of an Alum

Recovery of Elemental Copper from Copper (II) Nitrate

Estimation of Alcohol Content in Wine by Dichromate Oxidation followed by Redox Titration

EXPERIMENT 5: DIPEPTIDE RESEARCH PROJECT

Experiment #8 properties of Alcohols and Phenols

Distillation Experiment

This compound, which contains two carbon atoms with a C-OH structure on one end of the molecule is ethanol, commonly called ethyl alcohol.

Household Acids and Bases

POLYVINYL ALCOHOL. SYNONYMS Vinyl alcohol polymer, PVOH, INS No DEFINITION DESCRIPTION FUNCTIONAL USES CHARACTERISTICS

EXPERIMENT 6 (Organic Chemistry II) Identification of Ketones and Aldehydes

Chapter 22 Carbonyl Alpha-Substitution Reactions

Experiment 1: Colligative Properties

Organic Chemistry Calculations

Experiment 2: Recrystallization & Melting Point

ORGANIC COMPOUNDS IN THREE DIMENSIONS

Making Biodiesel from Virgin Vegetable Oil: Teacher Manual

MILESTONE. RotoSYNTH. Rotative Solid-Phase Microwave Reactor

To measure the solubility of a salt in water over a range of temperatures and to construct a graph representing the salt solubility.

Sulfa Antibiotics - Synthesis of Sulfanilamide

EXPERIMENT FIVE. Preparation of Cyclohexene from Cyclohexanol: an Elimination Reaction DISCUSSION

Transcription:

Experiment 1 Nucleophilic aromatic substitution Introduction S N Ar reactions are used on an industrial scale for the preparation of pharmaceuticals. Nucleophilic aromatic substitution (S N Ar) reactions offer a useful way to functionalize an aromatic ring. The high π electron density of an aromatic ring results in predominant reactivity towards electrophiles; however, if the aromatic ring is activated with electron withdrawing groups (EWG) ortho and/or para to a good leaving group, a nucleophilic substitution reaction is possible. Halogens are the most common leaving groups for S N Ar reactions and functional groups such as -NO 2, -SO 2 R, -NR 3, -CF 3 and -CN are electron withdrawing enough to render the aromatic ring susceptible to reaction with an electron-rich nucleophile, such as an amine. The two-step mechanism is supported by the isolation of many Meisenheimer salts. Evidence for a rate determining first step comes from the observation that fluoroaromatics undergo nucleophilic substitution much more rapidly than their iodo- counterparts, despite the fact that I - is a much better leaving group than F -. The reaction follows an addition-elimination two-step reaction sequence. It is generally accepted that the first step, in which a tetrahedral cyclohexadienyl anion called a Meisenheimer complex is formed, is the rate-determining step (rds). This is generated by the addition of the nucleophile to the carbon bearing the leaving group. Subsequent elimination of the halogen substituent (leaving group) leads to regeneration of the aromaticity in the ring. Thiocyanates are salts and esters of thiocyanic acid HSC N. They are some of the compounds responsible for the spicy taste in radishes and black mustard. In this experiment, one of three nucleophiles (potassium thiocyanate, ethylamine, or aniline) is used to substitute for the bromine on 1-bromo-2,4-dintrobenzene. The three possible products from the S N Ar with 1-bromo-2,4-dinitrobenzene are all highly-colored crystalline solids, and are as follows: 11

Experimental procedure Microwave Unit: MARS Procedure for 2,4-dinitrophenyl thiocyanate: Reagents used: The reactions are run using ethanol or a water ethanol mixture as the solvent. This makes it a clean reaction and the product is easy to isolate. 1-Bromo-2,4-dinitrobenzene is classified as an irritant. Potassium thiocyanate is a toxic compound. This reaction should not be attempted in a sealed reaction vessel without temperature control. HP-500 vessel as well as information on programming the MARS System. 1-Bromo-2,4-dinitrobenzene (0.296 mg, 1.20 mmol), potassium thiocyanate (0.467 mg, 4.80 mmol), ethanol (4.0 ml) and water (1.0 ml) are placed in an HP-500 Teflon microwave reaction vessel containing a magnetic stir bar. NOTE: The final volume must be at least 5 ml. The reaction vessel is inserted into the protective sleeve, fitted with the vessel top and load disk, and then placed into the vessel frame. The pre-set torque wrench is used to tighten the nut on top of the frame before placing it on the microwave turntable. Note the position the vessel occupies. The reaction control vessel (position #1) is connected to the temperature thermocouple and, if applicable, to the pressure sensor. The microwave is programmed using the ramp-to-temperature method to heat to 125 C over a 2-minute period and then held at this temperature for 20 minutes. The solution is then allowed to cool for 5 minutes, or until it is below 50 C before removing from the microwave unit. CAUTION: The vessel may still be hot to the touch. The vessel is vented by loosening the blue nut. It is then removed from the frame and its protective sleeve. The reaction mixture is cooled in an ice bath to initiate crystallization. Once crystallization is complete, the product can be collected by vacuum filtration and washed with cold solvent. The brightly colored crystalline 12

product can then be dried on a clay plate. When the product is dry, the melting point should be determined and compared to that in the literature. The crude product can be re-crystallized from 95% ethanol and characterized by IR, 1 H-NMR and/or 13 C-NMR spectroscopy. The purity can be determined by TLC using 40% ethyl acetate/hexanes as eluent. Procedure for 2,4-dinitro-N-ethylaniline: No water is added; ethanol is the only solvent used. 1-Bromo-2,4-dinitrobenzene is classified as an irritant. Ethylamine (70% aqueous) is flammable and corrosive. This reaction should not be attempted in a sealed reaction vessel without temperature control. HP-500 vessel as well as information on programming the MARS System. 1-Bromo-2,4-dinitrobenzene (0.298 mg, 1.20 mmol, 1 eq.), ethylamine (0.380 ml, 4.80 mmol), ethanol (4.0 ml) and water (1.0 ml) are placed in an HP-500 Teflon microwave reaction vessel containing a magnetic stir bar. NOTE: The final volume must be at least 5 ml. The reaction vessel is inserted in to the protective sleeve, fitted with the vessel top and load disk, and then placed into the vessel frame. The pre-set torque wrench is used to tighten the nut on top of the frame before placing it on the microwave turntable. Note the position the vessel occupies. The reaction control vessel (position #1) is connected to the temperature thermocouple and, if applicable, to the pressure sensor. The microwave is programmed using the ramp-to-temperature method to heat to 125 C over a 2-minute period and then held at this temperature for 5 minutes. The solution is then allowed to cool for 20 minutes, or until it is below 50 C before removing fromthe microwave unit. CAUTION: The vessel may still be hot to the touch. The vessel is vented by loosening the blue nut. It is then removed from the frame and its protective sleeve. The reaction mixture is cooled in an ice bath to initiate crystallization. Once crystallization is complete, the product can be collected by vacuum filtration and washed with cold solvent. The brightly colored crystalline product can then be dried on a clay plate. When the product is dry, the melting point should be determined and compared to that in the literature. The crude product can be re-crystallized from 95% ethanol and characterized by IR, 1 H-NMR and/or 13 C-NMR spectroscopy. The purity can be determined by TLC using 40% ethyl acetate/hexanes as eluent. 13

Procedure for 2,4-dinitrodiphenylamine: No water is added; ethanol is the only solvent used. 1-Bromo-2,4-dinitrobenzene and aniline are classified as irritants. Aniline is a toxic compound. This reaction should not be attempted in a sealed reaction vessel without temperature control. HP-500 vessel as well as information on programming the MARS System. 1-Bromo-2,4-dinitrobenzene (0.296 mg, 1.20 mmol), aniline (0.440 ml, 4.80 mmol), and ethanol (5.0 ml) are placed in an HP-500 Teflon microwave reaction vessel containing a magnetic stir bar. NOTE: The final volume must be at least 5 ml. The reaction vessel is inserted in to the protective sleeve, fitted with the vessel top and load disk, and then placed into the vessel frame. The pre-set torque wrench is used to tighten the nut on top of the frame before placing it on the microwave turntable. Note the position the vessel occupies. The reaction control vessel (position #1) is connected to the temperature thermocouple and, if applicable, to the pressure sensor. The microwave is programmed using the ramp-to-temperature method to heat to 125 C over a 2-minute period and then held at this temperature for 5 minutes. The solution is then allowed to cool for 20 minutes, or until it is below 50 C before removal from the microwave unit. CAUTION: The vessel may still be hot to the touch. The vessel is vented by loosening the blue nut. It is then removed from the frame and its protective sleeve. The reaction mixture is cooled in an ice bath to initiate crystallization. Once crystallization is complete, the product can be collected by vacuum filtration and washed with cold solvent. The brightly colored crystalline product can then be dried on a clay plate. When the product is dry, the melting point should be determined and compared to that in the literature. The crude product can be re-crystallized from 95% ethanol and characterized by IR, 1 H-NMR and/or 13 C-NMR spectroscopy. The purity can be determined by TLC using 40% ethyl acetate/hexanes as eluent. 14

Experimental procedure Microwave Unit: Discover Procedure for 2,4-dinitrophenyl thiocyanate: Reagents used: 1-Bromo-2,4-dinitrobenzene is classified as an irritant. Potassium thiocyanate is a toxic compound. This reaction should not be attempted in a sealed reaction vessel without temperature control. reaction vessel. 1-Bromo-2,4-dinitrobenzene (0.298 g, 1.20 mmol), potassium thiocyanate (0.467 g, 4.80 mmol), ethanol (2.5 ml) and water (0.5 ml) are added to a 10-mL glass microwave reaction vessel containing a stir bar. The reaction vessel is sealed with a cap and then placed into the microwave cavity. The pressure device is put in place on top of the reaction vessel and the unit programmed to heat the reaction mixture to 125 C and hold it for 5 minutes. After the reaction is complete and the vessel has cooled to below 50 C, the pressure device can be removed and the vessel may be taken from the microwave cavity. CAUTION: The tube may still be hot to the touch. The sealed reaction vessel and its contents are cooled in an ice bath to initiate crystallization. The brightly-colored crystalline product can be collected by vacuum filtration, washed with cold ethanol, and dried on a clay plate. When the product is dry, the melting point should be determined and compared to that in the literature. The crude product can be re-crystallized from 95% ethanol and characterized by IR, 1 H-NMR and/or 13 C-NMR spectroscopy. The purity can be determined by TLC using 40% ethyl acetate/hexanes as eluent. 16

Procedure for 2,4-dinitro-N-ethylaniline: No water is added; ethanol is the only solvent used. 1-Bromo-2,4-dinitrobenzene is classified as an irritant. Ethylamine (70% aqueous) is flammable and corrosive. This reaction should not be attempted in a sealed reaction vessel without temperature control. reaction vessel. 1-Bromo-2,4-dinitrobenzene (0.298 g, 1.20 mmol), ethylamine (0.380 ml, 4.80 mmol), and ethanol (3.0 ml) are added to a 10-mL glass microwave reaction vessel containing a stir bar. The reaction vessel is sealed with a cap and then placed into the microwave cavity. The pressure device is put in place on top of the reaction vessel and the unit programmed to heat the reaction mixture to 125 C and hold it for 5 minutes. After the reaction is complete and the vessel has cooled to below 50 C, the pressure device can be removed and the vessel may be taken from the microwave cavity. CAUTION: The tube may still be hot to the touch. The sealed reaction vessel and its contents are cooled in an ice bath to initiate crystallization. The brightly-colored crystalline product can be collected by vacuum filtration, washed with cold ethanol, and dried on a clay plate. When the product is dry, the melting point should be determined and compared to that in the literature. The crude product can be re-crystallized from 95% ethanol and characterized by IR, 1 H-NMR and/or 13 C-NMR spectroscopy. The purity can be determined by TLC using 40% ethyl acetate/hexanes as eluent. 17

Procedure for 2,4-dinitrodiphenylamine: No water is added; ethanol is the only solvent used. 1-Bromo-2,4-dinitrobenzene and aniline are classified as irritants. Aniline is a toxic compound. This reaction should not be attempted in a sealed reaction vessel without temperature control. reaction vessel. 1-Bromo-2,4-dinitrobenzene (0.298 g, 1.20 mmol), aniline (0.440 ml, 4.80 mmol), and ethanol (3.0 ml) are added to a 10-mL glass microwave reaction vessel containing a stir bar. The reaction vessel is sealed with a cap and then placed into the microwave cavity. The pressure device is put in place on top of the reaction vessel and the unit programmed to heat the reaction mixture to 125 C and hold it for 5 minutes. After the reaction is complete and the vessel has cooled to below 50 C, the pressure device can be removed and the vessel may be taken from the microwave cavity. CAUTION: The tube may still be hot to the touch. The sealed reaction vessel and its contents are cooled in an ice bath to initiate crystallization. The brightly-colored crystalline product can be collected by vacuum filtration, washed with cold ethanol, and dried on a clay plate. When the product is dry, the melting point should be determined and compared to that in the literature. The crude product can be re-crystallized from 95% ethanol and characterized by IR, 1 H-NMR and/or 13 C-NMR spectroscopy. The purity can be determined by TLC using 40% ethyl acetate/hexanes as eluent. 18

Lab Questions 1. Draw all the possible resonance structures for the Meisenheimer complex below. 2. The introduction lists a number of functional groups that are considered electron withdrawing. Explain why they are classified as electron withdrawing groups in the context of aromatic chemistry. 3. In the following reaction scheme, identify all of the following: nucleophile, leaving group, and electron withdrawing group. 4. Why is cold solvent used to wash your product rather than room temperature or hot solvent? 5. Which bromine in 1,2-dibromo-4-nitrobenzene would be substituted by a nucleophile? 19