پديدآورندگان :
Heshami Marouf m.heshami@iasbs.ac.ir Institute for Advanced Studies in Basic Sciences (IASBS), Zanjan , Kazemi Foad Institute for Advanced Studies in Basic Sciences (IASBS), Zanjan
چكيده فارسي :
The oxidation of alcohols to the corresponding carbonyl compounds is a key reaction in
organic synthesis. The selective oxidation of alcohols to aldehydes orketones is a very
important organic transformation, especially in preparing of some important precursors and
intermediates for drugs, fine chemicals, vitamins and fragrances [1]. Acyclic and cyclic
acetals of various carbonylcompounds were obtained in excellent yields under a mildreaction
condition in the presence of trialkyl orthoformateand a catalytic amount of
tetrabutylammonium tribromide(TBATB) in absolute alcohol [2]. In this work, we reported
aerobic photo oxidation of alcohols by TBATB to corresponding carbonyl compound at room
temperature. The carbonyl compound was characterized by 1HNMR,13CNMR, Gas
Chromatography (GC) and FT-IR. This method presented high yield, chemoselective, and
safe, operationally simple under mild reaction conditions, fast and cost-effective. Also, this
investigationshowed that we used light as a green and available source.