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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 905182생성일: 2026년 10월 25일

Hydrochloric Acid → (4R)-3-(S-Benzoyl-3-mercaptopropanoyl)-2-(2-thienyl)-4-thiazolidinecarboxylic acid

https://huagongshe.com/reaction/905182

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium CarbonateHCID 10340—
반응물Propanoyl chloride, 3-bromo-HCID 84944—
반응물(R)-2-Thiophen-2-ylthiazolidine-4-carboxylic acidHCID 6710826—
반응물Potassium thiobenzoateHCID 23681850—
용매WaterHCID 962—
생성물(4R)-3-(S-Benzoyl-3-mercaptopropanoyl)-2-(2-thienyl)-4-thiazolidinecarboxylic acidHCID 12915812—

반응 단계

10.6 g of (4R)-2-(2-thienyl)-4-thiazolidinecarboxylic acid and 10.6 g of sodium carbonate are dissolved in 100 ml of water and 8.6 g of 3-bromopropanoyl chloride is added dropwise while stirring under ice-cooling. After the addition, the mixture is stirred under ice-cooling for 2 hours. To this reaction solution, 8.8 g of potassium thiobenzoate is added and stirred at room temperature for 1 hour. The solution is acidified with dilute hydrochloric acid and the produced oil is extracted with ethyl acetate. The ethyl acetate layer is washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated in vacuo to give the titled compound, yield 11.6 g (57%), mp. 141°-143° C. (benzene), [α]D25 +107.7° (c=1.0, methanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04423054
출처 데이터셋uspto-grants-1983_12
ORD IDord-2b8e3795268d423c83ea5e5df9d61b41
출처 메모uspto-grants-1983_12