化工社化工社 化学情報印刷レポート · 研究参考用
Ethylene Glycol → Ethyl 2-methyl-1,3-dioxolane-2-propionate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethylene Glycol | HCID 174 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | Ethyl levulinate | HCID 10883 | — |
| 反応物 | Pyridinium.p-toluenesulfonate | HCID 22033616 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Ethyl 2-methyl-1,3-dioxolane-2-propionate | HCID 70332 | — |
反応手順
In a flask equipped by a Dean-Stark trap, a mixture of ethyl levulinate (28.83 g; 200 mmol), ethylene glycol (37.24 g; 600 mmol) and a catalytic amount of pyridinium para-toluenesulfonic acid in toluene (200 mL) was heated at reflux until the theoretical amount of water was distilled off. After cooling, the mixture was washed with a saturated solution of sodium hydrogenocarbonate. The basic layer was extracted with diethylether and the organics were combined, then washed with brine and water. The organic layer was dried over sodium sulphatesulphate and concentrated under reduced pressure to afford the ethyl 3-(2-methyl-1,3-dioxolan-2-yl)propanoate as a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08785638B2 |
| 出典データセット | uspto-grants-2014_07 |
| ORD ID | ord-ef41ac51bcf841e29afb641fc0b8899b |
| 出典メモ | uspto-grants-2014_07 |