戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1196407作成日:2026年10月27日

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

https://huagongshe.com/reaction/1196407

反応式

関与物質

役割名称HCID仕込み量
反応物Acetone CyanohydrinHCID 6406—
反応物TriethylamineHCID 8471—
反応物4-Chloro-2-nitrobenzoyl chlorideHCID 10867784—
反応物6,6-Dimethylpiperidine-2,4-dioneHCID 12695593—
溶媒DichloromethaneHCID 6344—
生成物3-(4-Chloro-2-nitrobenzoyl)-6,6-dimethylpiperidine-2,4-dioneHCID 1989819162.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05114461
出典データセットuspto-grants-1992_05
ORD IDord-cce4e7944be34b27b9fe87c1ed71c64c
出典メモuspto-grants-1992_05