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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1196407생성일: 2026년 10월 26일

Acetone Cyanohydrin → 3-(4-Chloro-2-nitrobenzoyl)-6,6-dimethylpiperidine-2,4-dione

https://huagongshe.com/reaction/1196407

반응식

참여 물질

역할이름HCID투입량
반응물Acetone CyanohydrinHCID 6406—
반응물TriethylamineHCID 8471—
반응물4-Chloro-2-nitrobenzoyl chlorideHCID 10867784—
반응물6,6-Dimethylpiperidine-2,4-dioneHCID 12695593—
용매DichloromethaneHCID 6344—
생성물3-(4-Chloro-2-nitrobenzoyl)-6,6-dimethylpiperidine-2,4-dioneHCID 1989819162.1%

반응 단계

A solution of 4-chloro-2-nitrobenzoyl chloride (4.4 g) in dry dichloromethane (5 ml) was added at 5°-10° C. to a stirred solution of 6,6-dimethylpiperidine-2,4-dione (2.8 g) and triethylamine (2.8 ml) in dry dichloromethane (50 ml) and the mixture was stirred at ambient temperature for 18 hours. Triethylamine (8.4 ml) and acetone cyanohydrin (0.4 ml) were added successively to the solution and the mixture was stirred at ambient temperature for 4 hours. The resulting solution was washed successively with 2N hydrochloric acid (25 ml) and water (3×25 ml), dried over sodium sulphate and evaporated under reduced pressure to give a yellow solid which was recrystallised from acetonitrile to give 3-(4-chloro-2-nitrobenzoyl)-6,6-dimethylpiperidine-2,4-dione (4 g), mp 162°-162.5° C., as a yellow crystalline solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05114461
출처 데이터셋uspto-grants-1992_05
ORD IDord-cce4e7944be34b27b9fe87c1ed71c64c
출처 메모uspto-grants-1992_05