化工社化工社 化学情報印刷レポート · 研究参考用
Ethyl 2-amino-3-sulfanylpropanoate → Ethyl 2-Amino-3-(2-furanylthio)propanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl 2-amino-3-sulfanylpropanoate | HCID 3297 | — |
| 反応物 | 2,5-Dihydro-2,5-dimethoxyfuran | HCID 78974 | — |
| 触媒 | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | Ethyl 2-Amino-3-(2-furanylthio)propanoate | HCID 20149579 | 31% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04730044 |
| 出典データセット | uspto-grants-1988_03 |
| ORD ID | ord-b2d631c393184639b9838869c6e2b4a4 |
| 出典メモ | uspto-grants-1988_03 |