Direct conversion of esters to aldehydes and ketones via piperazine amide under mild conditions

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초록

Aldehydes and ketones are basic, versatile intermediates used in organic synthesis. Various substituted aldehydes and ketones were directly prepared from carboxylic esters under mild conditions with excellent yields. The in situ generated aminolysis intermediate, piperazine-1,4-diylbis(phenylmethanone) amide, is readily reacted with commercial DIBALH and n-BuLi to obtain carbonyls in a one-pot reaction. The key amide intermediate was obtained in quantitative yield among the screened secondary amines. Hence, the formation of piperazine amide from the ester group, eliminated the utility of cryogenic temperatures and reduction proceeded under mild conditions. In addition, gram-scale preparation of aldehyde and ketone was reported in good yields.

키워드

aldehydediisobutylaluminum hydrideesterketonepiperazineMETHOXY-N-METHYLAMIDEST-BUTOXYALUMINUM HYDRIDEEFFICIENT REDUCING AGENTONE-POT SYNTHESISMORPHOLINE AMIDESREDUCTIONANALOGSDESIGN
제목
Direct conversion of esters to aldehydes and ketones via piperazine amide under mild conditions
저자
Kwak, Jae SeokJaladi, Ashok KumarAn, Duk Keun
DOI
10.1002/bkcs.12937
발행일
2025-02
유형
Article
저널명
Bulletin of the Korean Chemical Society
46
2
페이지
152 ~ 155