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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 401779생성일: 2026년 10월 24일

Triethylamine → 3-Chloro-4-({[3-chloro-4-(trifluoromethyl)benzyl]amino}carbonyl)benzenesulfonyl chloride

https://huagongshe.com/ko/reaction/401779

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Chloro-4-(chlorosulfonyl)benzoyl chlorideHCID 19814731—
반응물3-Chloro-4-(trifluoromethyl)benzylamineHCID 23512744—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물3-Chloro-4-({[3-chloro-4-(trifluoromethyl)benzyl]amino}carbonyl)benzenesulfonyl chlorideHCID 5773211640.7%

반응 단계

To a solution of 2-chloro-4-(chlorosulfonyl)benzoyl chloride (J. Org. Chem., 56,16, 1991, 4974) (300 mg, 0.877 mmol, 1 eq) in DCM (3 ml) was added 3-chloro-4-(trifluoromethyl)benzylamine (175 mg, 0.835 mmol, 0.95 eq) and Et3N (33 mg, 0.32 mmol, 0.37 eq) and the reaction mixture stirred at room temperature for 1 hour. The reaction mixture was diluted with ethyl acetate (10 ml), washed with water (10 ml), dried over sodium sulphate, filtered and evaporated. The crude material was purified by column chromatography eluting with ethyl acetate to yield the title compound (154 mg, 0.34 mmol, 39%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741934B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-d756446f2c68467997e93dcdcb194469
출처 메모uspto-grants-2014_06