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HRID 28668作成日:2026年10月24日

Aniline → 4-Anilino-3-nitrobenzoic acid

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

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物4-MethylmorpholineHCID 7972—
反応物4-Fluoro-3-nitrobenzoic acidHCID 67987—
溶媒2-MethoxyethanolHCID 8019—
生成物4-Anilino-3-nitrobenzoic acidHCID 3824366—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419995B2
出典データセットuspto-grants-2008_09
ORD IDord-117d740f4ce941b198f1a4abcf68544e
出典メモuspto-grants-2008_09