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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278161Generated: October 30, 2026

Benzaldehyde → 3-(3-Methoxypheny)-1-phenylpropanol

https://huagongshe.com/reaction/278161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactant1-Bromo-2-(3-methoxyphenyl)ethaneHCID 137450—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178490129HCID 178490129—
SolventTetrahydrofuranHCID 8028—
Product3-(3-Methoxypheny)-1-phenylpropanolHCID 14224733—

Reaction Steps

To a solution of benzaldehyde (920 μl, 9 mmol) in dry THF (20 mL) was added slowly a solution of 2-(3-methoxyphenyl) ethylmagnesium bromide prepared from 2-(3-methoxyphenyl) ethyl bromide (2.1 g. 9.77 mmol) and magnesium (300 mg, 12 mmol). The mixture was stirred at room temperature for ½ hour then quenched with saturated NH4Cl. The mixture was then extracted into EtOAc, washed with H2O, dried (Na2SO4), filtered and concentrated in vacuo, then purified by silica gel chromatography (30% EtOAc/Hexane) to provide the desired product as a colorless viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358985B1
Source datasetuspto-grants-2002_03
ORD IDord-3ee10c20dc3a44fabeb57aae702fd5f5
Source noteuspto-grants-2002_03