戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 400233作成日:2026年10月26日

Oxiranemethanol, 3-[(phenylmethoxy)methyl]- → 3-Allyl-4-(benzyloxy)-3-hydroxy-1-butanol

https://huagongshe.com/reaction/400233

反応式

関与物質

役割名称HCID仕込み量
反応物Oxiranemethanol, 3-[(phenylmethoxy)methyl]-HCID 3934498—
反応物HCID 178418473HCID 178418473—
溶媒TetrahydrofuranHCID 8028—
生成物3-Allyl-4-(benzyloxy)-3-hydroxy-1-butanolHCID 18944106—

反応条件

温度-40 °C

反応手順

A solution of 4-benzyloxy-2,3-epoxy-1-butanol (6.28 g, 32.37 mmol) in anhydrous tetrahydrofuran (75 mL) was added dropwise at -40° C. over a period of 45 minutes, to a 2M solution of allyl magnesium chloride (48.5 mL, 97 mmol) and tetrahydrofuran (50 mL). The solution was stirred at -40° C. for 1 hour, warmed to 0° C. and quenched by addition of aqueous ammonium chloride solution. The tetrahydrofuran layer was separated and the aqueous layer was extracted with ethyl acetate (three times). The combined organic extract was dried (magnesium sulfate), filtered and concentrated to obtain a mixture of compounds A and B.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05827868
出典データセットuspto-grants-1998_10
ORD IDord-757e5a1c8b554ab7918a14250606dd48
出典メモuspto-grants-1998_10