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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 327382생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/327382

반응식

참여 물질

역할이름HCID투입량
반응물EthanethiolHCID 6343—
반응물Sodium hydrideHCID 24758—
반응물4-Amino-5-chloro-2-methoxybenzoic acidHCID 81626—
용매DimethylformamideHCID 6228—
생성물4-Amino-5-chloro-2-hydroxybenzoic acidHCID 1488322283.4%

반응 조건

온도25 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05273972
출처 데이터셋uspto-grants-1993_12
ORD IDord-7efec71635e9487ead43743c726bc72a
출처 메모uspto-grants-1993_12