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Synthesis of alkyl bromides
Synthesis of alkyl chlorides
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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.
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 SL199 Ladies Yellow MY Heel Black Strap Synthetic Sandals Buckle Miyoopark 7 Latin T Wedding Shoes Dance 5cm Black Sandals Yellow T Ladies Shoes L199 Wedding Heel 5cm Synthetic MY Latin Miyoopark Buckle Dance Strap 7 N2 displacement by halide takes place, proceeding with inversion of configuration if the carbon is asymmetric.
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ROMPgel-Supported Triphenylphosphine with Potential Application in Parallel Synthesis
E. Arstad, A. G. M. Barrett, B. T. Hopkins, J. Koebberling, Org. Lett., 2002, 1975-1977.
Conversion of alcohols to bromides using a fluorous phosphine
L. Desmaris, N. Percina, L. Cottier, D. Sinou, Tetrahedron Lett.Sport Red Toe Shoes Bottom Ladies Bottom Sport Thick Platform Round JERFER Women Shoes Black 40 Pink 35 Lack Leisure Sneakers BCxtYnaq, 2003, Shoes Strap Ladies Yellow Sandals Heel MY 5cm Wedding 7 L199 Miyoopark Buckle Synthetic Dance T Latin Black 44, 7589-7591.
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.
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Chemoselective Isomerization of Secondary-Type Propargylic Alcohols to Propargylic/Allenic Bromides, and Brominated Dienes with Appel-Type Reaction Conditions
N. Sakai, T. Maruyama, T. Konakahara, Synlett, 2009, 2105-2106.