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HRID 327382作成日:2026年10月26日

Ethanethiol → 4-Amino-5-chloro-2-hydroxybenzoic acid

https://huagongshe.com/reaction/327382

反応式

関与物質

役割名称HCID仕込み量
反応物EthanethiolHCID 6343—
反応物Sodium hydrideHCID 24758—
反応物4-Amino-5-chloro-2-methoxybenzoic acidHCID 81626—
溶媒DimethylformamideHCID 6228—
生成物4-Amino-5-chloro-2-hydroxybenzoic acidHCID 1488322283.4%

反応条件

温度25 °C

反応手順

A cooled (5° C.) suspension of 60% sodium hydride oil dispersion (20.0 g, 0.50 mole) in anhydrous dimethylformamide (300 ml) under nitrogen was treated dropwise with ethyl mercaptan (18.7 g, 0.3 mole) while maintaining the reaction temperature below 15° C. The solution was stirred for 15 minutes at 25° C., cooled (5° C.), and treated in small portions with 4-amino-5-chloro-2-methoxybenzoic acid (40.33 g, 0.2 mole). The mixture was heated to 105°±5° C. for 4 hours, cooled, concentrated in vacuo to remove most of the dimethylformamide, then diluted with water (500 ml). The aqueous solution was extracted with methylene chloride (2×150 ml), then with ether (150 ml), acidified with concentrated HCl (55 ml), filtered, and the filter cake was washed with water and dried in vacuo in the presence of Drierite to provide a crude product. The product was recrystallized from tetrahydrofuran/hexane to yield 31.3 g (83%) of white solid, mp 192° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05273972
出典データセットuspto-grants-1993_12
ORD IDord-7efec71635e9487ead43743c726bc72a
出典メモuspto-grants-1993_12