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HRID 322057作成日:2026年10月27日

Dicyclohexylcarbodiimide → 3-Oxo-1-cyclohexenyl 2-chloro-3-(5-methoxymethylisoxazol-3-yl)-4-methylsulfonylbenzoate

https://huagongshe.com/reaction/322057

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物1,2-CyclohexanedioneHCID 13006—
反応物2-Chloro-3-(5-methoxymethylisoxazol-3-yl)-4-methylsulfonylbenzoic acidHCID 22009891—
溶媒DichloromethaneHCID 6344—
生成物3-Oxo-1-cyclohexenyl 2-chloro-3-(5-methoxymethylisoxazol-3-yl)-4-methylsulfonylbenzoateHCID 22009888—

反応手順

1.04 g (3.0 mmol) of 2-chloro-3-(5-methoxymethylisoxazol-3-yl)-4-methylsulfonylbenzoic acid are introduced into 50 ml of dichloromethane together with 0.37 g (3.3 mmol) of cyclohexanedione and treated with 0.68 g (3.3 mmol) of dicyclohexylcarbodiimide. After stirring at room temperature for 16 hours, the precipitate is filtered off with suction and the filtrate is washed with water. After the removal of the solvent, 1.22 g (92% of theory) of 3-oxo-1-cyclohexenyl 2-chloro-3-(5-methoxymethylisoxazol-3 yl)-4-methyl-sulfonylbenzoate are obtained as a yellowish, partly crystalline oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211216B1
出典データセットuspto-grants-2001_04
ORD IDord-b70296b47fef4bb4ba62f871f81db572
出典メモuspto-grants-2001_04