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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18898생성일: 2026년 10월 24일

Hydrochloric Acid → N-(2-benzoyl-4-chloro-phenyl)-4-iodo-benzenesulfonamide

https://huagongshe.com/ko/reaction/18898

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-Iodobenzenesulfonyl chlorideHCID 7399—
반응물2-Amino-5-chlorobenzophenoneHCID 12870—
용매PyridineHCID 1049—
용매TolueneHCID 1140—
생성물N-(2-benzoyl-4-chloro-phenyl)-4-iodo-benzenesulfonamideHCID 10028837—

반응 단계

To a magnetically stirred solution of 2-amino-5-chlorobenzophenone (1.62 g, 7.0 mmol) in dry pyridine (30 mL) was added dropwise a solution of pipsyl chloride in toluene (12 mL) and the reaction was stirred at ambient temperature. The reaction was added to cold (ice bath) 6M hydrochloric acid with stirring and the mixture was extracted with ethyl acetate (3×50 mL). The extracts were washed with water and with saturated aqueous NaCl. The organic layer was dried (MgSO4), filtered and concentrated to give a crystalline solid. The product was filtered, washed with hexane and dried (vacuum) to get white crystalline solid. 1H NMR (CDCl3) δ 9.63 (br s, 1H, NH), 7,75 (dm, 1H, J=8.8 Hz), 7.62 (tm, 1H, J=7.6 Hz), 7.56 (dm, 1H, J=7.6 Hz), 7.48 (m, 3H), 7.32 (m, 5H). MS: m/z 498.0 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741519B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b0a0b1bcdaaa45ae94632dc13858f9ea
출처 메모uspto-grants-2010_06