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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | Propanoyl chloride, 3-bromo- | HCID 84944 | — |
| 반응물 | (R)-2-Thiophen-2-ylthiazolidine-4-carboxylic acid | HCID 6710826 | — |
| 반응물 | Potassium thiobenzoate | HCID 23681850 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | (4R)-3-(S-Benzoyl-3-mercaptopropanoyl)-2-(2-thienyl)-4-thiazolidinecarboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04423054 |
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| 출처 데이터셋 | uspto-grants-1983_12 |
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| ORD ID | ord-2b8e3795268d423c83ea5e5df9d61b41 |
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| 출처 메모 | uspto-grants-1983_12 |
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