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Benzyl Alcohol → 2-Furancarboxylic acid, tetrahydro-, phenylmethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzyl Alcohol | HCID 244 | — |
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Tetrahydro-2-furancarbonyl chloride | HCID 551254 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 2-Furancarboxylic acid, tetrahydro-, phenylmethyl ester | HCID 11287208 | — |
反応手順
Tetrahydrofuroyl chloride (15.0 g, 112 mmol) was added dropwise to a cold solution of benzyl alcohol (10.9 g, 101 mmol) and pyridine (20.0 g, 253 mmol) in Et2O (200 mL). The solution was stirred at 0° for 40 minutes, then filtered to remove the side product pyridine hydrochloride. The filtrate was washed with 0.1M HCl (50 mL), saturated aqueous NaHCO3 (50 mL), and brine (50 mL), and then dried over MgSO4. Filtration and evaporation of the solvent gave a yellow oil, which was distilled. Benzyl tetrahydrofuroate was obtained as a colorless oil (21.1 g), b.p. 118° to 120° at 0.5 mm Hg.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05628980 |
| 出典データセット | uspto-grants-1997_05 |
| ORD ID | ord-1f9b60caca7c4d5cb481bbf00fbc0584 |
| 出典メモ | uspto-grants-1997_05 |