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The oxidation of six aliphatic aldehydes by tetraethylammonium chlorochromate (TEACC) in dimethyl sulfoxide (DMSO) leads to the formation of the corresponding carboxylic acids. The reaction is first order each in TEACC and the aldehyde. The reaction is catalysed by hydrogen ions. The hydrogen -ion dependence has the form: k obs ¼ a þ b½H þ . The oxidation of deuteriated acetaldehyde, MeCDO, exhibited a substantial primary kinetic isotope effect (k H yk D ¼ 5:83 at 298 K). The oxidation of acetaldehyde has been studied in 19 different organic solvents. The solvent effect has been analysed using Taft's and Swain's multiparametric equations. The rate constants correlate well with Taft's s* values; reaction constants being negative. A mechanism involving transfer of hydride ion has been suggested.

The synthetic potential of a new Cr(VI) reagent, viz., 1‐methylimidazolium chlorochromate, analogous to Corey's reagent‐PCC, has been examined. Anhydrous acetic acid has been found to catalyze the oxidation reaction.

Bei der Umsetzung mit N‐Bromsuccinimid (II) in feuchtem DMF entsteht aus Citronellol (I) das Keton (III).