関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | Methyl Acrylate | HCID 7294 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | (+)-Methyl lactate | HCID 637514 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | (2R)-4-methoxycarbonyl-2-methyltetrahydrofuran-3-one | HCID 54449678 | 37% |
反応手順
A solution of methyl (R)-(+)-lactate (30 g) in diethyl ether (60 ml) was added dropwise to a stirred mixture of sodium hydride (65%, 10.42 g) and diethyl ether (180 ml) which had been cooled to -35° C. The mixture was allowed to warm to 0° C. and stirred for 20 minutes. The mixture was evaporated. To the residue so obtained there was added a solution of methyl acrylate (29.2 ml) in DMSO (120 ml) which had been cooled to 10° C. The mixture was stirred in an ice-bath for 30 minutes and at ambient temperature for 2 hours. The mixture was poured into cold dilute (5%) aqueous sulphuric acid and extracted with diethyl ether. The organic phase was washed with a cold aqueous sodium bicarbonate solution and with brine, dried (MgSO4) and evaporated. The residue was distilled to give (2R)-4-methoxycarbonyl-2-methyltetrahydrofuran-3-one (16.5 g, 37%), b.p. 66°-68° C. (0.5 mm Hg), [alpha]20 =+55.3° (conc.=1.16 g per 100 ml of chloroform).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05482966 |
|---|
| 出典データセット | uspto-grants-1996_01 |
|---|
| ORD ID | ord-4dfdbc038b83474dbb86e11ebae6e988 |
|---|
| 出典メモ | uspto-grants-1996_01 |
|---|