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HRID 2559作成日:2026年10月24日

Bicarbonate Ion → rac-(1R,4S)-4-hydroxycyclopent-2-en-1-yl acetate

https://huagongshe.com/ja/reaction/2559

反応式

関与物質

役割名称HCID仕込み量
反応物Bicarbonate IonHCID 769—
反応物p-Toluenesulfonic acidHCID 6101—
反応物Carbonate IonHCID 19660—
反応物(+)-Acetic acid cis-4-(tetrahydro-pyran-2-yloxy)-cyclopent-2-enyl esterHCID 13623284—
溶媒EthanolHCID 702—
溶媒ChloroformHCID 6212—
生成物rac-(1R,4S)-4-hydroxycyclopent-2-en-1-yl acetateHCID 1015410375%

反応手順

Dissolve (-)-acetic acid cis-4-(tetrahydro-pyran-2-yloxy)-cyclopent-2-enyl ester (192 mg, 0.85 mmol, prepared in example 11) in ethanol (1.5 mL) and treat with p-toluenesulfonic acid (11.7 mg). Stir the reaction at room temperature for 2 hours. Add carbonate or bicarbonate to neutralize the reaction mixture and concentrate under vacuum. Purify the residue by chromatography (silica gel, 3 g, 1.5×3 cm column, 33% ethyl acetate/hexane, 80 mL), to provide the title compound (90 mg, 75% yield, 91% ee), [α]20 D =-66.1°, (c=0.63, 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-4b9e268c96f04af98cb23843c3e81f50
出典メモuspto-grants-1998_03