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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18872생성일: 2026년 10월 23일

Benzenesulfonyl chloride, 3,4-dichloro- → N-(2-benzoyl-4-chloro-phenyl)-3,4-dichloro-benzenesulfonamide

https://huagongshe.com/ko/reaction/18872

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chloride, 3,4-dichloro-HCID 7383—
반응물2-Amino-5-chlorobenzophenoneHCID 12870—
생성물N-(2-benzoyl-4-chloro-phenyl)-3,4-dichloro-benzenesulfonamideHCID 11247684—

반응 단계

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 115 mg of (2-amino-5-chloro-phenyl)-phenyl-methanone and 123 mg of 3,4-Dichloro-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 7.25 (d, 1H, J=8.8 Hz), 7.36-39 (m, 3H), 7.43-47 (m, 3H), 7.53 (dd, 1H, J=8.8 Hz, 2.4 Hz), 7.61 (m, 1H), 7.65 (m, 1H), 7.73 (d, 1H, J=8.8 Hz), 9.56 (s, 1H). MS: m/z 440.7 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741519B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b0bd93ef82ba4277b77e5c9ef6beaa1a
출처 메모uspto-grants-2010_06