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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662568Generated: October 25, 2026

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

https://huagongshe.com/reaction/1662568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium bis(2-methoxyethoxy)aluminiumhydrideHCID 21584525—
Reactant1-(3-(Benzyloxy)phenyl)but-2-yn-1-olHCID 57705992—
SolventDiethyl EtherHCID 3283—
Product(E)-1-(3-(Benzyloxy)phenyl)but-2-en-1-olHCID 5770712486%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030354B2
Source datasetuspto-grants-2011_10
ORD IDord-aa32dbddf9e44890a239782237168f65
Source noteuspto-grants-2011_10