After completing this section, you should be able to
- write an equation to describe the industrial preparation of ethylene oxide.
- list two important industrial uses of ethylene oxide.
- write an equation to describe the normal laboratory preparation of an epoxide.
- identify the epoxide produced from the reaction of a given alkene with a peroxyacid.
- identify the alkene, the reagent, or both, needed to prepare a given epoxide.
- write an equation to describe the preparation of an epoxide from an alkene via a halohydrin.
Make certain that you can define, and use in context, the key term below.
- epoxide (oxirane)
Epoxides (also known as oxiranes) are three-membered ring structures in which one of the vertices is an oxygen and the other two are carbons. Epoxides behave differently than other ethers due to the strain created by the three-membered ring.
The most important and simplest epoxide is ethylene oxide which is prepared on an industrial scale by catalytic oxidation of ethylene by air. Ethylene oxide is used as an important chemical feedstock in the manufacturing of ethylene glycol, which is used as antifreeze, liquid coolant and solvent. In turn, ethylene glycol is used in the production of polyester and polyethylene terephthalate (PET) the raw material for plastic bottles.
Nomenclature of Epoxides
The name ethylene oxide is not systematic but common. Epoxides are systematically named as an oxirane ring system much like the other cyclic ethers discussed in Section 18.1. The oxygen is numbered in the 1 position.
Synthesis of Epoxides
As discussed in Section 8-7, epoxides are typically prepared by the reaction of an alkene and a peroxycarboxylic acid (RCO3H), such as meta-chloroperbenzoic acid (MCPBA). The peroxycarboxylic acid has the unique property of having an electropositive oxygen atom on the CO3H group. The reaction is initiated by the electrophilic oxygen atom reacting with the nucleophilic carbon-carbon double bond. The mechanism involves a concerted reaction with a four-part, circular transition state. The result is that the originally electropositive oxygen atom ends up in the oxacyclopropane ring and the CO3H group becomes CO2H.
The oxygen addition to the alkene is a syn addition and is stereospecific. The substituents of a cis-alkene will appear in the cis configuration on the epoxide ring. Likewise, Substituents of a trans-alkene will appear in the trans configuration on the epoxide ring. During this reaction the sp2 hybridized carbons of the alkene are converted to sp3 hybridized carbons in the epoxide. Thus, there is the possibility of two new chiral carbons forming in the epoxide product. In most cases, epoxidation of an alkene will product a mixture of enantiomers in the product, due to the electrophilic oxygen being able to attack from above or below the plane of the alkene. One major exception is the epoxidation of symmetrical cis-alkene which produces a meso compound product.
Treatment of an alkene with X2 & H2O creates a halohydrin (Section 8-3). When a halohydrin is treated with a base the alcohol is deprotonated to from an alkoxide. This causes an intramolecular Williamson ether synthesis to produce an epoxide along with the elimination of HX. Note, that this reaction generally forms a mixture of enantiomeric products unless a meso compound is produced.
What reagents would you use to perform the following transformation?
Lindlar's catalyst reduces alkynes to cis/Z alkenes. This stereochemistry is retained after epoxidation.
Predict the products of the following reactions:
Contributors and Attributions
Prof. Steven Farmer (Sonoma State University)
John D. Robert and Marjorie C. Caserio (1977) Basic Principles of Organic Chemistry, second edition. W. A. Benjamin, Inc. , Menlo Park, CA. ISBN 0-8053-8329-8. This content is copyrighted under the following conditions, "You are granted permission for individual, educational, research and non-commercial reproduction, distribution, display and performance of this work in any format."