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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5376생성일: 2026년 10월 24일

2-Chloroethyl methyl sulfide → 4-Amino-5-chloro-2-[2-(methylthio)ethoxy]benzoic acid

https://huagongshe.com/ko/reaction/5376

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloroethyl methyl sulfideHCID 10965—
반응물Sodium hydrideHCID 24758—
반응물4-Amino-5-chloro-2-hydroxybenzoic acidHCID 14883222—
용매DimethylformamideHCID 6228—
생성물4-Amino-5-chloro-2-[2-(methylthio)ethoxy]benzoic acidHCID 1910840557%

반응 조건

온도25 °C

반응 단계

A cooled (5° C.) suspension of 60% sodium hydride oil dispersion (0.52 g, 13 mmoles) in anhydrous dimethylformamide (15 mL) under nitrogen was treated in portions with 4-amino-5-chloro-2-hydroxybenzoic acid (0.94 g, 5 mmoles), stirred for 15 minutes at 25° C., treated with (2-chloroethyl)methyl sulfide (1.66 g, 15 mmoles), and heated to 100° C. for 18 hours. The solution is cooled, concentrated in vacuo, and added to water (25 mL). The aqueous solution is extracted with ether, and the extract is dried (MgSO4), concentrated in vacuo, taken up in 50% aqueous ethanol (50 mL), treated with potassium hydroxide (5.0 g), and refluxed for one hour. The mixture is concentrated, diluted with water to 75 mL total volume, extracted with ether, and acidified to pH 3 with concentrated HCl. The precipitate is filtered, washed with water, air dried, and recrystallized from ethyl acetate to afford 0.74 g (57%) of product as fine voluminous white needles, mp 137.5°-139.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244907
출처 데이터셋uspto-grants-1993_09
ORD IDord-4a61892e548641678c1f2f77ac5daff8
출처 메모uspto-grants-1993_09