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HRID 280259作成日:2026年10月24日

N,N-Dimethylaniline → 6-Chloro-2-[(3-chloro-4-methoxyphenyl)amino]-3-nitrobenzoic acid

https://huagongshe.com/ja/reaction/280259

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DimethylanilineHCID 949—
反応物3-Chloro-4-methoxyanilineHCID 21441—
反応物2,6-Dichloro-3-nitrobenzoic acidHCID 350623—
溶媒ChloroformHCID 6212—
生成物6-Chloro-2-[(3-chloro-4-methoxyphenyl)amino]-3-nitrobenzoic acidHCID 13588347—

反応手順

A mixture of 30 g of 3-chloro-4-methoxyaniline, 18.9 g of 2,6-dichloro-3-nitrobenzoic acid, and 150 ml N,N-dimethylaniline was heated at 100° under nitrogen for 24 hours. The reaction mixture was dissolved in chloroform and washed with dilute ammonium hydroxide. After the aqueous layer was washed with chloroform, it was acidified and the resulting orange solid was collected to provide 6-chloro-2[(3-chloro-4-methoxyphenyl)amino]-3-nitrobenzoic acid, mp 222°-228° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04588730
出典データセットuspto-grants-1986_05
ORD IDord-2b9a38beeb7c47feb5cac4c6de898dbd
出典メモuspto-grants-1986_05