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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 322057생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/322057

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1,2-CyclohexanedioneHCID 13006—
반응물2-Chloro-3-(5-methoxymethylisoxazol-3-yl)-4-methylsulfonylbenzoic acidHCID 22009891—
용매DichloromethaneHCID 6344—
생성물3-Oxo-1-cyclohexenyl 2-chloro-3-(5-methoxymethylisoxazol-3-yl)-4-methylsulfonylbenzoateHCID 22009888—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06211216B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-b70296b47fef4bb4ba62f871f81db572
출처 메모uspto-grants-2001_04