Lagerblom Kalle, Wrigstedt Pauli, Keskiväli Juha, Parviainen Arno, Repo Timo
Department of Chemistry, University of Helsinki, A.I. Virtasen aukio 1, P.O. Box 55, 00014, Helsinki, Finland.
Chempluschem. 2016 Nov;81(11):1160-1165. doi: 10.1002/cplu.201600240. Epub 2016 Jul 28.
A method for aerobic alcohol oxidation catalysed by Fe(NO ) /2,2'-bipyridine/TEMPO has allowed highly selective conversion of primary alcohols into either aldehydes or carboxylic acids in one-step. The oxidation of primary alcohols proceeded selectively to aldehydes, as TEMPO was present in the reaction. Nevertheless, the aldehydes were further oxidized into carboxylic acids as the reaction time was extended. Detailed investigation of the reaction suggested, that the deoxygenation of TEMPO into TMP enabled the auto-oxidation of aldehydes to carboxylic acids, which was initially inhibited in the presence of TEMPO. The procedure was also efficient in oxidation of secondary alcohols when TEMPO was replaced by the less sterically hindered ABNO.
一种由Fe(NO₃)₃/2,2'-联吡啶/TEMPO催化的需氧醇氧化方法,可实现伯醇一步高选择性转化为醛或羧酸。当反应体系中存在TEMPO时,伯醇选择性氧化为醛。然而,随着反应时间延长,醛会进一步氧化为羧酸。对该反应的详细研究表明,TEMPO脱氧生成TMP使得醛能自动氧化为羧酸,而在TEMPO存在时这一过程最初受到抑制。当用空间位阻较小的ABNO取代TEMPO时,该方法对仲醇的氧化也很有效。