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HRID 1662568作成日:2026年10月26日

Sodium bis(2-methoxyethoxy)aluminiumhydride → (E)-1-(3-(Benzyloxy)phenyl)but-2-en-1-ol

https://huagongshe.com/reaction/1662568

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium bis(2-methoxyethoxy)aluminiumhydrideHCID 21584525—
反応物1-(3-(Benzyloxy)phenyl)but-2-yn-1-olHCID 57705992—
溶媒Diethyl EtherHCID 3283—
生成物(E)-1-(3-(Benzyloxy)phenyl)but-2-en-1-olHCID 5770712486%

反応条件

温度0 °C

反応手順

To a cold solution of sodium bis(2-methoxyethoxy)aluminum hydride (65+ wt. % in toluene) (available from Aldrich) (14.8 mL, 49.1 mmol) in ether (60 mL) was added a solution of 93.A (6.20 g, 24.6 mmol) in ether (30 mL) dropwise under nitrogen at 0° C. The mixture was stirred for 5 minutes at 0° C., the cooling bath was removed, and stirring was continued for 3 hours at room temperature. The reaction was carefully quenched at 0° C. with EtOAc, diluted with saturated aqueous Rochelle salt, and extracted with additional EtOAc. The combined organics were washed with water and brine, dried (MgSO4), and concentrated. The crude product was purified by silica gel flash chromatography (0-20% EtOAc/hexane) to afford 93.B (5.37 g, 86% yield) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08030354B2
出典データセットuspto-grants-2011_10
ORD IDord-aa32dbddf9e44890a239782237168f65
出典メモuspto-grants-2011_10