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HRID 851737作成日:2026年10月26日
Hydrochloric Acid → (4R)-3-(S-Benzoyl-3-mercaptopropanoyl)-2-(2-thienyl)-4-thiazolidinecarboxylic acid
https://huagongshe.com/reaction/851737
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sodium Carbonate | HCID 10340 | — |
| 反応物 | Propanoyl chloride, 3-bromo- | HCID 84944 | — |
| 反応物 | (R)-2-Thiophen-2-ylthiazolidine-4-carboxylic acid | HCID 6710826 | — |
| 反応物 | Potassium thiobenzoate | HCID 23681850 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | (4R)-3-(S-Benzoyl-3-mercaptopropanoyl)-2-(2-thienyl)-4-thiazolidinecarboxylic acid | HCID 12915812 | — |
反応手順
10.8 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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04386096 |
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| 出典データセット | uspto-grants-1983_05 |
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| ORD ID | ord-c48840041f4b492e917f672990787e51 |
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| 出典メモ | uspto-grants-1983_05 |
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