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Water → (1S,4R)-4-(Benzyloxy)cyclopent-2-en-1-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Chloroform | HCID 6212 | — |
| 反応物 | Lithium hydroxide, monohydrate | HCID 168937 | — |
| 反応物 | (-)-Acetic acid cis-4-benzyloxy-cyclopent-2-enyl ester | HCID 86752290 | — |
| 溶媒 | Methanol tetrahydrofuran water | HCID 21892291 | — |
| 生成物 | (1S,4R)-4-(Benzyloxy)cyclopent-2-en-1-ol | HCID 15812323 | 92.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05728899 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-91b9cd4f6514451c9af570b41fa98ef5 |
| 出典メモ | uspto-grants-1998_03 |