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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1741782생성일: 2026년 10월 27일

2-Bromobenzoic acid → 2-bromo-N-(4-nitrophenyl)benzamide

https://huagongshe.com/reaction/1741782

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromobenzoic acidHCID 6940—
반응물4-NitroanilineHCID 7475—
반응물Thionyl ChlorideHCID 24386—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물2-bromo-N-(4-nitrophenyl)benzamideHCID 521255587%

반응 조건

온도80 °C

반응 단계

Thionyl chloride (120.5 g) was added to a stirred mixture of 2-bromobenzoic acid (194.0 g) in toluene (500 mL) and N,N-dimethylformamide (DMF) (5 mL) and the mixture heated at 80° C. for 4 hours. The solution was cooled to 20° C. and added slowly to a solution of 4-nitroaniline (133.1 g) in toluene (500 mL) and N-methylpyrrolidone (NMP) (120 mL), maintaining the temperature of the reaction mixture between 20°-25° C. The reaction mixture was then stirred for 24 hours, during which time a solid precipitated. Water (360 mL) was added with rigorous stirring. The suspended solid was collected by filtration, and washed successively with water, toluene and acetonitrile to give 2-bromo-N-(4-nitrophenyl)benzamide (B) as a solid, in 87% yield; m.p. 200°-202° C.; NMR (d6 -DMSO): 7.4-7.8(m, 7H), 8.0(d, 2H), 8.3(d, 2H), 11.5(br s, 1H). This material was used without further purification in step (ii).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05334718
출처 데이터셋uspto-grants-1994_08
ORD IDord-9a8d4332b7774a00bccd89f4509f1f03
출처 메모uspto-grants-1994_08