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2,3-Epoxybutane is an
organic compound In chemistry, organic compounds are generally any chemical compounds that contain carbon- hydrogen or carbon-carbon bonds. Due to carbon's ability to catenate (form chains with other carbon atoms), millions of organic compounds are known. Th ...
with the formula CH3CH(O)CHCH3. It is an
epoxide In organic chemistry, an epoxide is a cyclic ether () with a three-atom ring. This ring approximates an equilateral triangle, which makes it strained, and hence highly reactive, more so than other ethers. They are produced on a large scale ...
. The compound exists as three stereoisomers, a pair of enantiomers and the meso isomer. All are colorless liquids.


Preparation and reactions

2,3-Epoxybutane is prepared from
2-butene But-2-ene is an acyclic alkene with four carbon atoms. It is the simplest alkene exhibiting ''cis''/''trans''-isomerism (also known as (''E''/''Z'')-isomerism); that is, it exists as two geometric isomers ''cis''-but-2-ene ((''Z'')-but-2-ene) and ...
via the
chlorohydrin In organic chemistry a halohydrin (also a haloalcohol or β-halo alcohol) is a functional group in which a halogen and a hydroxyl are bonded to adjacent carbon atoms, which otherwise bear only hydrogen or hydrocarbyl groups (e.g. 2-chloroethan ...
:Heinz Gräfje, Wolfgang Körnig, Hans-Martin Weitz, Wolfgang Reiß, Guido Steffan, Herbert Diehl, Horst Bosche, Kurt Schneider and Heinz Kieczka "Butanediols, Butenediol, and Butynediol" in ''Ullmann's Encyclopedia of Industrial Chemistry'', 2019, Wiley-VCH, Weinheim. :CH3CH=CHCH3 + HOCl → CH3CH(OH)CH(Cl)CH3 :CH3CH(OH)CH(Cl)CH3 → CH3CH(O)CHCH3 + HCl A common reaction is its hydration to
2,3-butanediol 2,3-Butanediol is the organic compound with the formula (CH3CHOH)2. It is classified as a ''vic''-diol (glycol). It exists as three stereoisomers, a chiral pair and the meso isomer. All are colorless liquids. Applications include precursors to ...
. Many such
ring-opening reaction A cyclic compound (or ring compound) is a term for a compound in the field of chemistry in which one or more series of atoms in the compound is connected to form a ring. Rings may vary in size from three to many atoms, and include examples where ...
s have been reported.


References

{{DEFAULTSORT:Epoxybutane, 2,3- Epoxides