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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28668생성일: 2026년 10월 23일

Aniline → 4-Anilino-3-nitrobenzoic acid

https://huagongshe.com/ko/reaction/28668

반응식

참여 물질

역할이름HCID투입량
반응물AnilineHCID 6115—
반응물4-MethylmorpholineHCID 7972—
반응물4-Fluoro-3-nitrobenzoic acidHCID 67987—
용매2-MethoxyethanolHCID 8019—
생성물4-Anilino-3-nitrobenzoic acidHCID 3824366—

반응 단계

4-Fluoro-3-nitrobenzoic acid (0.27 mol), an aniline (0.32 mol) and NMM (32.5 mL) in 2-methoxyethanol (750 mL) were stirred at reflux under argon for 24 h. The suspension was concentrated under reduced pressure and the residue was sonicated with 1M HCl (aq) over 1.5 h. The resultant orange solid was isolated by filtration, washed with water dried, then sonicated with t-butyl methyl ether, isolated by filtration and dried. Where necessary, the product was further purified by recrystallisation to yield the 4-anilino-3-nitrobenzoic acid: e.g. 4-(3-bromophenyl amino)-3-nitrobenzoic acid. (In some cases, for example with heteroaromatic anilines, NMN may be omitted from the reaction mixture).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419995B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-117d740f4ce941b198f1a4abcf68544e
출처 메모uspto-grants-2008_09