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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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium CarbonateHCID 10340—
反応物Propanoyl chloride, 3-bromo-HCID 84944—
反応物(R)-2-Thiophen-2-ylthiazolidine-4-carboxylic acidHCID 6710826—
反応物Potassium thiobenzoateHCID 23681850—
溶媒WaterHCID 962—
生成物(4R)-3-(S-Benzoyl-3-mercaptopropanoyl)-2-(2-thienyl)-4-thiazolidinecarboxylic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04386096
出典データセットuspto-grants-1983_05
ORD IDord-c48840041f4b492e917f672990787e51
出典メモuspto-grants-1983_05