Appel Reaction

The reaction of triphenylphosphine and tetrahalomethanes (CCl₄, CBr₄) with alcohols is a ready method to convert an alcohol to the corresponding alkyl halide under mild conditions. The yields are normally high.

This reaction is somewhat similar to the Mitsunobu Reaction, where the combination of a phosphine, a diazo compound as a coupling reagent, and a nucleophile are used to invert the stereochemistry of an alcohol or displace it.

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Mechanism of the Appel Reaction

The reaction proceeds by activation of the triphenylphosphine by reaction with the tetrahalomethane, followed by attack of the alcohol oxygen at phosphorus to generate an oxyphosphonium intermediate. The oxygen is then transformed into a leaving group, and an S_N2 displacement by halide takes place, proceeding with inversion of configuration if the carbon is asymmetriC.

Recent Literature

Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling

ROMPgel-Supported Triphenylphosphine with Potential Application in Parallel Synthesis

Conversion of alcohols to bromides using a fluorous phosphine

Stoichiometric bromotrichloromethane in acetonitrile can replace solvent quantities of carbon tetrachloride in the synthesis of gem-dichloroalkenes from aldehydes in the presence of triphenylphosphine. Similarly, bromotrichloromethane in dichloromethane can be used for the Appel reaction of benzyl alcohols to form benzyl chlorides at r.t., which is commonly carried out in refluxing carbon tetrachloride.

The facile preparation of alkenyl metathesis synthons

Halogenation through Deoxygenation of Alcohols and Aldehydes

Catalysis of Phosphorus(V)-Mediated Transformations: Dichlorination Reactions of Epoxides Under Appel Conditions

Dehydration of Amides to Nitriles under Conditions of a Catalytic Appel Reaction

Chemoselective Isomerization of Secondary-Type Propargylic Alcohols to Propargylic/Allenic Bromides, and Brominated Dienes with Appel-Type Reaction Conditions