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HRID 36561作成日:2026年10月25日

Acetone Cyanohydrin → 2-(4-Methylsulphonyl-2-nitrobenzoyl)-5,5-dimethylcyclohexane-1,3-dione

https://huagongshe.com/reaction/36561

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DimedoneHCID 31358—
反応物4-(Methanesulfonyl)-2-nitrobenzoyl chlorideHCID 14800186—
溶媒DichloromethaneHCID 6344—
生成物2-(4-Methylsulphonyl-2-nitrobenzoyl)-5,5-dimethylcyclohexane-1,3-dioneHCID 1993713948.8%

反応手順

A solution of 4-methylsulphonyl-2-nitrobenzoyl chloride (9.62 g) in dry dichloromethane (50 ml) was added to a stirred solution of triethylamine (5.6 ml) and 5,5-dimethylcyclohexane-1,3-dione (5 g) in dry dichloromethane (70 ml) during 30 minutes and the reaction mixture stirred at ambient temperature for 4 hours. Triethylamine (15.3 ml) and acetone cyanohydrin (0.5 ml) were added successively and the reaction mixture stirred at ambient temperature for 18 hours. The reaction mixture was washed successively with 2N hydrochloric acid (2×50 ml) and water (2×50 ml), dried over magnesium sulphate and evaporated under reduced pressure to give a yellow glass which was recrystallised from methanol (20 ml) to give 2-(4-methylsulphonyl-2-nitrobenzoyl)-5,5-dimethylcyclohexane-1,3-dione (6.4 g), m.p. 156.5°-158° C., as a yellow crystalline solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05416061
出典データセットuspto-grants-1995_05
ORD IDord-d58fcbdd740644d9af498b7e9b6eb406
出典メモuspto-grants-1995_05