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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18885생성일: 2026년 10월 25일

4-t-Butylbenzenesulfonyl chloride → 4-tert-Butyl-N-[4-chloro-2-(4-fluoro-benzoyl)-phenyl]benzenesulfonamide

https://huagongshe.com/reaction/18885

반응식

참여 물질

역할이름HCID투입량
반응물4-t-Butylbenzenesulfonyl chlorideHCID 139882—
반응물4-Chloro-2-(4-fluorobenzoyl)anilineHCID 10955955—
생성물4-tert-Butyl-N-[4-chloro-2-(4-fluoro-benzoyl)-phenyl]benzenesulfonamideHCID 11305378—

반응 단계

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously desribed using 125 mg of (2-Amino-5-chloro-phenyl)-(4-fluoro-phenyl)-methanone and 116 mg of 4-tert-butyl-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 1.21 (s, 9H), 7.09 (t, 2H, J=NMR 8.8 Hz), 7.29 (m, 3H), 7.43-7.50 (m, 3H), 7.59 (m, 2H), 7.77 (d, 1H, J=8.8 Hz), 9.72 (s, 1H). MS: m/z 446.0 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741519B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b977198e06e948ea953f7d2ce406537b
출처 메모uspto-grants-2010_06