Dehydrohalogenation

Dehalogenation to give an alkene.

Dehydrohalogenation is an chemical reaction that involves removal of (elimination of) a hydrogen halide from a substrate. The reaction is usually associated with the synthesis of alkenes, but it has wider applications.

Dehydrohalogenation from alkyl halides

Traditionally, alkyl halides are substrates for this dehydrohalogenations. The alkyl halide must be able to form an alkene, thus methyl and benzy halides are not suitable substrates. Aryl halides are also unsuitable. Upon treatment with strong base, chlorobenzene dehydrohalogenates to give phenol via a benzyne intermediate.

Base-promoted reactions

When treated with a strong base many alkyl chlorides convert to corresponding alkene.^[1] It is also called a β-Elimination reaction and is a type of elimination reaction. Zaitsev's rule helps to predict regioselectivity for this reaction type. Some examples are shown below:

{\begin{aligned}{\ce {{\underset {EthylChloride}{^{\beta }CH3-^{\alpha }CH2Cl}}+KOH}}\ &{\ce {->{\underset {Ethene}{CH2=CH2}}+{KCl}+H2O}}\\{\ce {{\underset {1-Chloropropane}{CH3-CH2-CH2Cl}}+KOH}}\ &{\ce {->{\underset {Propene}{CH3-CH=CH2}}+{KCl}+H2O}}\\{\ce {{\underset {2-Chloropropane}{CH3-CHCl-CH3}}+KOH}}\ &{\ce {->{\underset {Propene}{CH3-CH=CH2}}+{KCl}+H2O}}\end{aligned}}

Here ethyl chloride reacts with potassium hydroxide dissolved in ethanol, giving ethene. Likewise, 1-chloropropane and 2-chloropropane give propene.

In general, the reaction of haloalkane with potassium hydroxide can compete with an S_N2 nucleophilic substitution reaction by OH⁻ a strong, unhindered nucleophile. Alcohols are however generally minor products. Often dehydrohalogenations employ strong bases such as potassium tert-butoxide ([CH₃]₃CO⁻ K⁺).

Thermal cracking

On an industrial scale, base-promoted dehydrohalogenations as described above are disfavored. The disposal of the alkali halide salt is problematic. Instead thermally-induced dehydrohalogenations are preferred. One example is provided by the production of vinyl chloride by heating 1,2-dichloroethane:^[2]

CH₂Cl-CH₂Cl → CH₂=CHCl + HCl

The resulting HCl can be reused in oxychlorination reaction.

Thermally induced dehydrofluorinations are employed in the production of fluoroolefins and hydrofluoroolefins. One example is the preparation of 1,2,3,3,3-pentafluoropropene from 1,1,2,3,3,3-hexafluoropropane:

CF₂HCH(F)CF₃ → CHF=C(F)CF₃ + HF

Formation of epoxides

Chlorohydrins, compounds with the connectivity R(HO)CH-CH(Cl)R', undergo dehydrochlorination to give epoxides. This reaction is employed industrially to produce millions of tons of propylene oxide annually from propylene chlorohydrin:^[3]

CH₃CH(OH)CH₂Cl + KOH → CH₃CH(O)CH₂ + H₂O + KCl

External links

Dehydrohalogenation

References

↑ March, Jerry (1985), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (3rd ed.), New York: Wiley, ISBN 0-471-85472-7
↑ M. Rossberg et al. "Chlorinated Hydrocarbons" in Ullmann’s Encyclopedia of Industrial Chemistry, 2006, Wiley-VCH, Weinheim. doi:10.1002/14356007.a06_233.pub2
↑ Nijhuis, T. Alexander; Makkee, Michiel; Moulijn, Jacob A.; Weckhuysen, Bert M. "The Production of Propene Oxide: Catalytic Processes and Recent Developments" Industrial & Engineering Chemistry Research 2006, volume 45, 3447-3459. doi:10.1021/ie0513090

Authority control	GND: 4149015-0

This article is issued from Wikipedia - version of the 10/23/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.