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HRID 242017作成日:2026年10月25日

Allyl bromide → Methyl 2-(allyloxy)propanoate

https://huagongshe.com/reaction/242017

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl bromideHCID 7841—
反応物Methyl LactateHCID 11040—
反応物Sodium hydrideHCID 24758—
反応物Sodium BicarbonateHCID 516892—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-(allyloxy)propanoateHCID 13971956—

反応条件

温度0 °C

反応手順

(±)-Methyl-2-hydroxypropanoate (7.6 g, 74 mmol) was dissolved in tetrahydrofuran (100 mL), cooled to 0° C. and treated with sodium hydride (3.6 g, 60% dispersion, 89 mmol, 1.2 equiv) portionwise over 45 minutes. The mixture was warmed to ambient temperature, stirred for 30 minutes, and then cooled to 0° C. Allyl bromide (8.4 mL, 96 mmol, 1.3 equiv) was added, the mixture was warmed to ambient temperature and stirred for an additional 14 hours. Sodium bicarbonate (10 mL, aqueous saturated) was added slowly and the mixture was stirred for 30 minutes before being poured into water (500 mL). The aqueous layer was extracted with ethyl acetate (2×300 mL) and the combined organic extracts were washed once with brine, dried with sodium sulfate, filtered and concentrated in vacuo, providing the titled compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653079B2
出典データセットuspto-grants-2014_02
ORD IDord-d4ecf825aa5b4d4e89202ad8f730cded
出典メモuspto-grants-2014_02