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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 505671생성일: 2026년 10월 25일

Methanesulfonyl chloride → N-[2-bromo-5-(trifluoromethyl)phenyl]methanesulfonamide

https://huagongshe.com/reaction/505671

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물2-Bromo-5-(trifluoromethyl)benzenamineHCID 67989—
용매PyridineHCID 1049—
생성물N-[2-bromo-5-(trifluoromethyl)phenyl]methanesulfonamideHCID 5943090452%

반응 단계

To a solution of 2-bromo-5-trifluoromethylaniline (3.18 g, 13.25 mmol) in pyridine (18 ml) was added methanesulfonyl chloride (1.03 ml, 13.25 mmol) and the mixture was stirred for 6 hours at room temperature. The solvent was removed in vacuo and the residue was diluted with chloroform. The organic layer was washed with water, 1N hydrochloric acid, a saturated sodium hydrogen carbonate solution and saturated brine and dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by recrystallization to give the subject compound (2.18 g, 52%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07781479B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-5888ddb31d474185be9e29694440c5d9
출처 메모uspto-grants-2010_08