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HRID 2556作成日:2026年10月24日

Water → (1S,4R)-4-(Benzyloxy)cyclopent-2-en-1-ol

https://huagongshe.com/ja/reaction/2556

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物ChloroformHCID 6212—
反応物Lithium hydroxide, monohydrateHCID 168937—
反応物(-)-Acetic acid cis-4-benzyloxy-cyclopent-2-enyl esterHCID 86752290—
溶媒Methanol tetrahydrofuran waterHCID 21892291—
生成物(1S,4R)-4-(Benzyloxy)cyclopent-2-en-1-olHCID 1581232392.8%

反応手順

Dissolve (-)-acetic acid cis-4-benzyloxy-cyclopent-2-enyl ester (158 mg, 0.68 mmol, prepared in example 17) in THF/methanol/water (1.5/0.5/0.5 mL). Add lithium hydroxide monohydrate (0.75 mmol) with stirring. After stirring for about 2 hours at room temperature, dilute the reaction with water (10 mL) and extract with tert-butyl methyl ether. Combine the organic phases, dry over anhydrous magnesium sulfate, filter and concentrate under vacuum. Purify the residue by flash chromatography (silica gel, 2 g, 20% ethyl acetate/hexane, 1.5×2.5 cm column) to provide the title compound (120 mg, 92% yield), [α]20D =+5.0°, (C=0.93, chloroform).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728899
出典データセットuspto-grants-1998_03
ORD IDord-91b9cd4f6514451c9af570b41fa98ef5
出典メモuspto-grants-1998_03