化学
酒精氧化
烯丙基重排
催化作用
酒
有机化学
盐(化学)
丙酮
分子氧
氧气
氧化还原
氯化物
烷基
作者
Shengming Ma,Jinxian Liu,Suhua Li,Bo Chen,Jiajia Cheng,Jinqiang Kuang,Yu Liu,Baoqiang Wan,Yuli Wang,Juntao Ye,Qiong Yu,Weiming Yuan,Shichao Yu
标识
DOI:10.1002/adsc.201100033
摘要
Abstract Oxidation of alcohols is a fundamental transformation related to our daily life. Traditional approaches with at least one stoichiometric amount of oxidants are expensive and cause serious environmental burdens. There are many reports on the aerobic oxidation of simple alcohols such as alkyl or phenyl carbinols and allylic alcohols, which used oxygen or air as the environmentally benign oxidant forming water as the only by‐product. However, no such protocol has been reported for allenols and propargylic alcohols. Thus, it still highly desirable to develop efficient room temperature oxidations of alcohols with a wide scope including allenols and propargylic alcohols. In this paper, an efficient and clean aerobic oxidation of so far the widest spectrum of alcohols using 1 atm of oxygen or air, producing aldehydes/ketones at room temperature in fairly high isolated yields mostly within a couple of hours is described. It is interesting to observe that the reaction has been efficiently expedited by a catalytic amount of sodium chloride in easily recoverable 1,2‐dichloroethane. A mechanism involving NO and NO 2 has been proposed based on the results of the control experiments and GC‐MS studies of the in‐situ formed gas phase of the reaction mixture.
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