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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27450생성일: 2026년 10월 25일

Ethyl chloroformate → 3-Ethoxycarbonylaminothiophenol

https://huagongshe.com/reaction/27450

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroformateHCID 10928—
반응물3-AminothiophenolHCID 31577—
용매Ethyl AcetateHCID 8857—
생성물3-EthoxycarbonylaminothiophenolHCID 23342978—

반응 단계

12 ml of ethyl chloroformate are added dropwise to a solution of 25 g of 3-aminothiophenol in 150 ml of ethyl acetate at 50°, under gentle reflux. 50 ml of ethyl acetate are added and the reaction mixture is boiled under reflux for 5 minutes, cooled to 40° and filtered with suction. The filtrate is evaporated to dryness and the oily evaporation residue is chromatographed on silica gel using toluene as the solvent. 3-Ethoxycarbonylaminothiophenol is obtained by evaporating the eluate. 10 g of this product are mixed with 8 g of ethyl acetoacetate and the mixture is added dropwise to 153 g of polyphosphoric acid at 90°. The mixture is warmed for 2 hours at an internal temperature of 95° and the hot reaction mixture is poured into 2 liters of ice-water, the resulting mixture is stirred for 30 minutes and the precipitate which has separated out is filtered off with suction. 2-Methyl-7-ethoxycarbonylamino-4-oxo-4H- 1-benzothiopyran is thus obtained and after recrystallisation from 70 ml of ethanol this melts at 216°-218°. 15.6 g of this product are refluxed with 28.7 ml of sulfuric acid and 52 ml of acetic acid for 5 hours. The reaction mixture is poured into 500 ml of ice-water and the resulting mixture is neutralised with sodium hydroxide solution. 2-Methyl-7-amino-4-oxo-4H-1-benzothiopyran with a melting point of 165°-169° is obtained and this can be purified via the hydrochloride and then melts at 172°-175°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04221806
출처 데이터셋uspto-grants-1980_09
ORD IDord-0595e43ec12a47869061e474a7857d44
출처 메모uspto-grants-1980_09