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HRID 22060作成日:2026年10月26日

Benzaldehyde → 1-Hydroxy-2-methyl-1-phenyl-3-pentanone

https://huagongshe.com/reaction/22060

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物Ethyl ketoneHCID 7288—
生成物1-Hydroxy-2-methyl-1-phenyl-3-pentanoneHCID 54601772%

反応条件

温度-78 °C

反応手順

50 mmol (5.1 ml) of benzaldehyde are added at -78° C. to the manganous enolate of diethyl ketone, prepared by the procedure described above. After stirring for 10 seconds at -78° C., the reaction medium is hydroIyzed by the dropwise addition of a saturated solution of (NH4)2SO4. After decantation, filtration on hyflo-supercel and evaporation of the solvents under vacuum, 5-phenyl-5-hydroxy-4-methylpentan-3-one is isolated by low pressure liquid chromatography on 15 μm silica gel using cyclohexane/ethyl acetate (90/10) as the eluent. Yield=72%. Erythro/threo=61/39.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05426201
出典データセットuspto-grants-1995_06
ORD IDord-eb2ffed42db34070991af4f46a60fd88
出典メモuspto-grants-1995_06