This alternative reduction involves heating a carbonyl compound with finely divided, amalgamated zinc in a hydroxylic solvent (often an aqueous mixture) containing a mineral acid such as HCl. The mercury alloyed with the zinc does not participate in the reaction, it serves only to provide a clean active metal surface.
The mechanism of Clemmensen reduction is not fully understood; intermediacy of radicals are implicated. Clemmensen reduction is complementary to Wolff-Kishner reduction, which also converts aldehydes and ketones to hydrocarbons, in that the former is carried out in strongly acidic conditions and the latter in strongly basic conditions.
- Clemmensen, E. Ber. Dtsch. Chem. Ges. 1913, 46, 1837–1843.
- Clemmensen, E. Ber. Dtsch. Chem. Ges. 1914, 47, 51–63.
- Clemmensen, E. Ber. Dtsch. Chem. Ges. 1914, 47, 681–687.