戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 568892作成日:2026年10月25日

Ethyl 2-amino-3-sulfanylpropanoate → Ethyl 2-Amino-3-(2-furanylthio)propanoate

https://huagongshe.com/reaction/568892

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl 2-amino-3-sulfanylpropanoateHCID 3297—
反応物2,5-Dihydro-2,5-dimethoxyfuranHCID 78974—
触媒4-Toluenesulfonyl chlorideHCID 7397—
溶媒AcetonitrileHCID 6342—
生成物Ethyl 2-Amino-3-(2-furanylthio)propanoateHCID 2014957931%

反応手順

To 16.25 g (125 mmol) of 2,5-dimethoxy-2,5-dihydrofuran and 23.20 g (125 mmol) of ethyl 2-amino-3-mercaptopropanoate in 100 ml dry acetonitrile was added approximately 0.15 g of tosyl chloride. The mixture was stirred 1 hour at room temperature under nitrogen during which time complete solution was attained which became very dark. The mixture was concentrated in vacuo, taken up in ethyl acetate, then extracted with aqueous NaHCO3 solution followed by saturated NaCl solution. The organic portion was dried over MgSO4, filtered then concentrated to 50 ml. The concentrate was then chromatographed to give 8.35 g (31.0%) of the title compound as a dark oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04730044
出典データセットuspto-grants-1988_03
ORD IDord-b2d631c393184639b9838869c6e2b4a4
出典メモuspto-grants-1988_03