STEP 5: ESTRONE-3-METHYL ETHER-17-ETHYLENE KETAL. Li / NH 3 (l) 1. Procedure

Similar documents
Recovery of Elemental Copper from Copper (II) Nitrate

PREPARATION AND PROPERTIES OF A SOAP

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

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

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

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

Isolation of Caffeine from Tea

DYES AND DYEING 2003 by David A. Katz. All rights reserved. Permission for classroom use provided original copyright is included.

Experiment 5 Preparation of Cyclohexene

Paper Chromatography: Separation and Identification of Five Metal Cations

Experiment 8 Synthesis of Aspirin

Experiment 8 Preparation of Cyclohexanone by Hypochlorite Oxidation

ISOLATION OF CAFFEINE FROM TEA

Physical and Chemical Properties and Changes

Determination of a Chemical Formula

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

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

PHYSICAL SEPARATION TECHNIQUES. Introduction

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

Hands-On Labs SM-1 Lab Manual

Experiment #7: Esterification

EXPERIMENT 7 Reaction Stoichiometry and Percent Yield

Steam Distillation of Lemongrass Oil

Distillation Experiment

Dry Ice Color Show Dry Ice Demonstrations

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

14 Friedel-Crafts Alkylation

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

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

CHEMICAL REACTIONS OF COPPER AND PERCENT YIELD KEY

SEPARATION OF A MIXTURE OF SUBSTANCES LAB

Experiment 5: Column Chromatography

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

Preparation of an Alum

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

Extraction: Separation of Acidic Substances

Desalination of Sea Water E7-1

Reaction of Magnesium with Hydrochloric Acid (Gas Laws) Chemicals Needed:

Table 1. Common esters used for flavors and fragrances

PECTINS. SYNONYMS INS No. 440 DEFINITION DESCRIPTION. FUNCTIONAL USES Gelling agent, thickener, stabilizer, emulsifier CHARACTERISTICS

Apparatus error for each piece of equipment = 100 x margin of error quantity measured

# 12 Condensation Polymerization: Preparation of Two Types of Polyesters

Separation by Solvent Extraction

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

#9 Condensation Polymerization: Preparation of Nylon 6/10

SODIUM CARBOXYMETHYL CELLULOSE

COMMON LABORATORY APPARATUS

Experiment 7: Titration of an Antacid

Acid Base Titrations

Synthesis of Isopentyl Acetate

Standard Operating Procedure

Dissolving of sodium hydroxide generates heat. Take care in handling the dilution container.

Synthesis of Aspirin and Oil of Wintergreen

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

Experiment 1: Colligative Properties

Acid-Base Extraction.

Synthesis of tetraamminecopper(ii) sulfate, [Cu(NH 3 ) 4 ]SO 4 The reaction for making tetraamminecopper(ii) sulfate and some molar masses are:

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

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

Laboratory procedures in polymer chemistry

Basics of Laboratory Safety: Chem 5a Lab 2003

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

Non-polar hydrocarbon chain

The Grignard Reaction. Preparation of Benzoic Acid

8.9 - Flash Column Chromatography Guide

Making Biodiesel from Virgin Vegetable Oil: Teacher Manual

Physical Properties of a Pure Substance, Water

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

Organic Chemistry Lab Experiment 4 Preparation and Properties of Soap

Separation and Identification of Plant Pigments Dr. Gergens - SD Mesa College

1. The Determination of Boiling Point

oxidize 4-Cholesten-3-one

PURIFICATION TECHNIQUES

Thin Layer and Column Chromatography

General Chemistry I (FC, 09-10) Lab #3: The Empirical Formula of a Compound. Introduction

The Properties of Water (Instruction Sheet)

PREPARATION FOR CHEMISTRY LAB: COMBUSTION

Properties of Acids and Bases

CH243: Lab 4 Synthesis of Artificial Flavorings by Fischer Esterification

The Molar Mass of a Gas

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

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

METHOD 3510C SEPARATORY FUNNEL LIQUID-LIQUID EXTRACTION

Experiment 12- Classification of Matter Experiment

EDTA Titrations 1: Standardization of EDTA and Analysis of Zinc in a Supplement Tablet. by Professor David Cash. September, 2008

#10 Condensation Polymerization: Preparation of Nylon 6/6

Santa Monica College Chemistry 11

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

Experiment 8 - Double Displacement Reactions

SYNTHESIS AND ANALYSIS OF A COORDINATION COMPOUND OF COPPER

Determination of calcium by Standardized EDTA Solution

DNA SPOOLING 1 ISOLATION OF DNA FROM ONION

Mixtures and Pure Substances

CHEMISTRY 338 THE SYNTHESIS OF LIDOCAINE

Agarose Gel Electrophoresis with Food Color- Teacher Guide

Chapter 5, Lesson 3 Why Does Water Dissolve Salt?

Chapter 3: Separating Mixtures (pg )

Fractional Distillation and Gas Chromatography

Syllabus OC18 Use litmus or a universal indicator to test a variety of solutions, and classify these as acidic, basic or neutral

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

Transcription:

STEP 5: ESTRNE-3-METYL ETER-17-ETYLENE KETAL 3 C Li / N 3 (l) 3 C C 3 C 3 1. Procedure At least 24 hours in advance: Fill a 250-mL, 3-necked round-bottomed flask equipped with a stirbar with 50 ml acetone. Mark the solvent level with a wax pencil (note 1), decant the acetone, air dry (note 2), then oven dry the flask, stirbar, and a coldfinger condenser overnight. Also dry a 100-mL round-bottomed flask. As quickly as possible, assemble the warm reaction apparatus as shown in Figure 5, omitting the cannula and the 100 ml round-bottomed flask. The 3-necked flask is fitted with the cold-finger condenser in the middle neck, a septum on a side neck, and a vacuum adapter on the other neck. Cool the apparatus under a stream of dry nitrogen. When cool, submerge the flask as deeply as possible in a dry ice-acetone bath. Also fill the cold-finger trap with dry ice and acetone (note 3). With nitrogen flowing, carefully turn on the ammonia tank so that the gas begins to condense in the dry ice-cooled flask (note 4). When approximately 50 ml of ammonia has condensed, stop the ammonia flow while maintaining nitrogen flow. Disconnect the ammonia tank, replacing the vacuum adapter on the side neck with another septum. Briefly remove the septum on either side neck and add lithium metal (10 equiv, in small pieces). Caution: Before handling 18

lithium metal, see note 5. Replace the septum, stop the nitrogen flow, and stir until all the metal dissolves. The reaction solution should be deep blue. Cool an oven-dried, septum-sealed 100-mL, round-bottomed flask and cannula under a stream of dry nitrogen by blowing nitrogen in through a needle and out through the cannula. When cool, remove the septum briefly to add the starting material, 3- methoxy-1,3,5(10),8(9)-estratetraene-17-ethylene ketal. Replace the septum, purge further with dry nitrogen, then add dry TF by syringe (sol n ~ 0.04 M). Swirl the flask gently to dissolve the starting material. Slowly transfer this solution by cannula to the cold solution of lithium in liquid ammonia (note 6). When the transfer is complete, quantitate the addition with more dry TF (5 ml). During the addition, add dry ice to the condenser and cooling bath as necessary. The reaction should be complete after 1 hour. Because an excess of lithium was used, the reaction solution should remain deep blue. If the color fades, add more lithium. To quench the excess lithium, remove the septum and add isoprene (about 0.5 ml) by pipette; the blue color should rapidly dissipate (note 7). Remove the condenser and the cooling bath to allow the ammonia to evaporate. When ammonia can no longer be detected (note 8), dilute the reaction mixture with an equal amount of ether. Wash sequentially with small portions of 5% Cl (1x) and distilled water (2x). Dry the organic layer over sodium sulfate, filter, and evaporate the solvent on the rotary evaporator. The resulting oily product may solidify under vacuum. Take a TLC of this crude product. Purify the crude reaction product via column chromatography. 19

2. Notes 1. Check that the solvent level mark is not acetone-soluble. 2. Do not put glassware wet with acetone in the oven; the oven could explode. 3. Fill only about 2/3 of the way. Do not let acetone overflow the trap. 4. Ammonia gas (bp 33 C) is strongly basic and corrosive. It is extremely irritating to the airway, eyes, and skin. Avoid breathing vapors. Wear goggles or safety glasses. Do not wear contact lenses in the laboratory, ever, but especially not when handling ammonia. Wear gloves and long sleeves to prevent skin exposure. 5. Caution: Lithium, like sodium and potassium, reacts violently with water to form hydrogen. The heat generated in this reaction is sufficient to ignite the hydrogen gas thus produced. In the presence of organic solvents, this could start a terrible fire. Fires involving alkali metals are considered class D fires, and cannot be extinguished by most ordinary fire extinguishers. Lithium wire is stored in mineral oil to minimize exposure to water in the air. To safely transport and weigh the metal, cut off one piece of wire and immediately place it in a beaker of dry hexane. At the scale, remove the wire from the beaker with forceps, briefly shake to dry, and weigh quickly. (Since such a large excess of lithium is used, getting an exact amount is not important. Try to get close to the required amount.) Put the wire back into the hexane beaker to return to the hood, where it can be cut into smaller pieces for the reaction. Dispose of excess lithium metal in a metal beaker filled with dry methanol. Lithium reacts much less violently with alcohols than with water. When the lithium has reacted completely with methanol, the solution can be poured into the liquid waste container. Do not place lithium waste in a solid waste container, trash can, or sink. rganic solvents which may have accidentally been poured into the sink could ignite when the lithium reacts with water. 20

6. To regulate the flow of the starting material solution through the cannula and into the ammonia solution, inject dry nitrogen from a 50-mL plastic syringe into the 100- ml flask. This gives more control over the flow rate than an active nitrogen stream. 7. Isoprene boils at 34 C and has a pungent odor. When not in the freezer, it should be kept on ice and in the hood. 8. Test for ammonia by holding a piece of moistened p paper over the neck of the flask. 3. Characterization and Report Determine the yield of product. If the product has solidified, determine its melting point. Characterize the product by IR and 1 and 13 C NMR. Tabulate and assign the spectral data. List the TLC conditions used and the Rf values of starting material and product. 21

22