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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18896생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/18896

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물p-Bromobenzenesulfonyl chlorideHCID 7396—
반응물2-Amino-5-chlorobenzophenoneHCID 12870—
용매WaterHCID 962—
용매PyridineHCID 1049—
용매Ethyl AcetateHCID 8857—
생성물N-(2-benzoyl-4-chloro-phenyl)-4-bromo-benzenesulfonamideHCID 333475798.4%

반응 단계

2-Amino-5-chlorobenzophenone (5.33 g, 23 mmol) was dissolved in 100 mL pyridine and stirred at room temperature. 4-Bromobenzenesulfonyl chloride (6.17 g, 24.1 mmol) was added and the mixture was stirred overnight. The mixture was poured in a steady stream into 350 mL vigorously stirring chilled 6M HCl which resulted in the precipitation of a reddish oil. The solution was diluted with 100 mL EtOAc and 200 mL H2O, shaken in a separating funnel and the aqueous layer discarded. The organics were dried and reduced in vacuo to yield title compound (10.2 g, 98%). 1H NMR (400 MHz, CDCl3): δ 7.34 (m, 5H), 7.43-7.48 (m, 5H), 7.62 (t, 1H), 7.74 (d, 1H), 9.62 (s, 1H). MS: m/z=449.9 (M++1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741519B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-26c50f35ca01425f953f3b1789ffe2e9
출처 메모uspto-grants-2010_06