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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 443701생성일: 2026년 10월 24일

m-(Trifluoromethyl)benzamide → 5-(alpha,alpha,alpha-Trifluoro-m-Tolyl)-1,3,4-Oxathiazol-2-One

https://huagongshe.com/ko/reaction/443701

반응식

참여 물질

역할이름HCID투입량
반응물m-(Trifluoromethyl)benzamideHCID 74535—
반응물(Chlorothio)formyl chlorideHCID 75990—
용매Ethyl AcetateHCID 8857—
생성물5-(alpha,alpha,alpha-Trifluoro-m-Tolyl)-1,3,4-Oxathiazol-2-OneHCID 1226011086.3%

반응 단계

α,α,α-Trifluoro-m-toluamide (82.7 g, 0.437 mol) and chlorocarbonylsulfenyl chloride (86 g, 0.667 mol, 53% excess) were reacted under the conditions of Example 2 for 0.5 hours. The light yellow residue was dissolved in ethyl acetate and cooled to -78°. The white precipitate was filtered and washed with hexane to yield 93.14 g (0.377 mol, 86.2%) of white solid, m.p. 85°-86.5°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04261728
출처 데이터셋uspto-grants-1981_04
ORD IDord-745498c25ccc40d08310b90c6e84aa74
출처 메모uspto-grants-1981_04