Geminal halide hydrolysis is an organic reaction. The reactants are geminal dihalides with a water molecule or a hydroxide ion. The reaction yields ketones from secondary halides[1][2] or aldehydes from primary halides.[3][4]
Reaction mechanism
editThe first part of the reaction mechanism consists of an ordinary nucleophilic aliphatic substitution to produce a gem-halohydrin:
- RCH(Cl)2 + KOH RCH(OH)Cl + KCl
The remaining halide is a good leaving group and this enables the newly created hydroxy group to convert into a carbonyl group by expelling the halide:
- RCH(OH)Cl Rearrangement gives R-CHO + HCl
Variations
editOther functional groups can undergo similar hydrolysis reactions. For instance, geminal trihalides (e.g. benzotrichloride) can be partially hydrolyzed to acyl halides (e.g. benzoyl chloride) in a similar way.[5] Further hydrolysis yields carboxylic acids.
See also
editReferences
edit- ^ Marvel, C. S.; Sperry, W. M. (1928). "Benzophenone". Organic Syntheses. 8: 26. doi:10.15227/orgsyn.008.0026.
- ^ Pond, F. J.; O. P., Maxwell; G. M., Norman (1899). "The Action of Sodium Methylate Upon Dibromides of Propenyl-Compounds and of Unsaturated Ketones". Journal of the American Chemical Society. 22 (11): 955–967. doi:10.1021/ja02061a002.
- ^ Bill, J. C.; Tarbell, D. S. (1954). "o-Phthalaldehyde". Organic Syntheses. 34: 82. doi:10.15227/orgsyn.034.0082.
- ^ Buck, Johannes S.; Zimmermann, F. J. (1938). "Protocatechualdehyde". Organic Syntheses. 18: 75. doi:10.15227/orgsyn.018.0075.
- ^ Rossberg, Manfred; Lendle, Wilhelm; Pfleiderer, Gerhard; Tögel, Adolf; Dreher, Eberhard-Ludwig; Langer, Ernst; Rassaerts, Heinz; Kleinschmidt, Peter; Strack, Heinz; Cook, Richard; Beck, Uwe; Lipper, Karl-August; Torkelson, Theodore R.; Löser, Eckhard; Beutel, Klaus K.; Mann, Trevor (2006). "Chlorinated Hydrocarbons". Ullmann's Encyclopedia of Industrial Chemistry: 139. doi:10.1002/14356007.a06_233.pub2. ISBN 3527306730.
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