戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 374935作成日:2026年10月25日

Sulfuric Acid → (2R)-4-methoxycarbonyl-2-methyltetrahydrofuran-3-one

https://huagongshe.com/reaction/374935

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Methyl AcrylateHCID 7294—
反応物Sodium hydrideHCID 24758—
反応物(+)-Methyl lactateHCID 637514—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Diethyl EtherHCID 3283—
生成物(2R)-4-methoxycarbonyl-2-methyltetrahydrofuran-3-oneHCID 5444967837%

反応条件

温度-35 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05482966
出典データセットuspto-grants-1996_01
ORD IDord-4dfdbc038b83474dbb86e11ebae6e988
出典メモuspto-grants-1996_01