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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 378485생성일: 2026년 10월 24일

2,4,5-Trichlorobenzenesulfonyl chloride → 2,4,5-Trichloro-N-(4-bromo-3-methyl-5-isoxazolyl)benzenesulfonamide

https://huagongshe.com/ko/reaction/378485

반응식

참여 물질

역할이름HCID투입량
반응물2,4,5-Trichlorobenzenesulfonyl chlorideHCID 27575—
반응물4-Bromo-3-methylisoxazol-5-amineHCID 10487519—
생성물2,4,5-Trichloro-N-(4-bromo-3-methyl-5-isoxazolyl)benzenesulfonamideHCID 1861728667%

반응 단계

2,4,5-Trichloro-N-(4-bromo-3-methyl-5-isoxazolyl)benzenesulfonamide was prepared from 5-amino-4-bromo-3-methylisoxazole and 2,4,5-trichlorobenzenesulfonyl chloride according to the procedures described in Example 30. The crude product was purified by recrystallization from ethyl acetate/hexanes to give a crystalline solid, m.p. 179-182° C., yield 67%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06030991
출처 데이터셋uspto-grants-2000_02
ORD IDord-3e3c6d3cebdb48c893139c026fd35837
출처 메모uspto-grants-2000_02