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Ethyl Thioglycolate → 5-(Carbethoxymethylthio)-1-(2-furyl)-1-pentanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl Thioglycolate | HCID 12185 | — |
| 反応物 | Sodium ethoxide | HCID 2723922 | — |
| 反応物 | 5-Chloro-1-(2-furyl)-1-pentanol | HCID 20292579 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-(Carbethoxymethylthio)-1-(2-furyl)-1-pentanol | HCID 20292574 | — |
反応手順
To a stirred, refluxing mixture of 76 g of ethyl mercaptoacetate, 79.5 g of 5-chloro-1-(2-furyl)-1-pentanol (Example 55), and 10 ml of 1.5 M sodium ethoxide in ethanol is added an additional 300 ml of 1.5 M sodium ethoxide during 15 minutes. The resulting mixture is stirred at reflux for 3 hours, cooled, and concentrated to remove most of the ethanol. The residue is partitioned with ether and water. The ether phase is washed with brine and dried over potassium carbonate. The solution is concentrated, diluted with xylene, and again concentrated to give an oil, pmr spectrum (CDCl3):δ3.24 (singlet, --S--CH2CO2C2H5) and 4.70 (triplet, CH2CHOH).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04243817 |
| 出典データセット | uspto-grants-1981_01 |
| ORD ID | ord-8aa1321754ac49dcb35ed01487bba8f2 |
| 出典メモ | uspto-grants-1981_01 |