Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 223705생성일: 2026년 10월 26일
Hydrochloric Acid → (4R)-3-(S-Benzoyl-3-mercaptopropanoyl)-2-(2-hydroxyphenyl)-4-thiazolidinecarboxylic acid
https://huagongshe.com/reaction/223705
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | (4R)-2-(2-hydroxyphenyl)-1,3-thiazolidine-4-carboxylic acid | HCID 2825745 | — |
| 반응물 | HCID 13013918 | HCID 13013918 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | (4R)-3-(S-Benzoyl-3-mercaptopropanoyl)-2-(2-hydroxyphenyl)-4-thiazolidinecarboxylic acid | HCID 12915688 | — |
반응 단계
11.3 g of (4R)-2-(2-hydroxyphenyl)-4-thiazolidinecarboxylic acid and 13.2 g of triethylamine are dissolved in 200 ml of dehydrated acetone and 11.7 g of S-benzoyl-3-mercaptopropanoyl chloride is added dropwise while stirring under ice-cooling. After the addition, the mixture is stirred under ice-cooling for 1 hour. 4 N Hydrochloric acid in ether is added to this mixture and the precipitate is filtered. The filtrate is concentrated in vacuo and the obtained oil is dissolved in ethyl acetate, washed with 2 N hydrochloric acid and saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated to dryness in vacuo to give the titled compound, yield 12 g (58%), mp. 100.5°-101° C. (dec.) (ethyl acetatebenzene), [α]D26 +130.8° (c=1.0, methanol).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04356183 |
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| 출처 데이터셋 | uspto-grants-1982_10 |
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| ORD ID | ord-f17ad56466724b708907331eafcc099d |
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| 출처 메모 | uspto-grants-1982_10 |
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