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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798371Generated: November 1, 2026

Water → (4-Bromophenyl)(4-chlorophenyl)methanol

https://huagongshe.com/reaction/1798371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-BromobenzaldehydeHCID 70741—
ReactantHCID 178478191HCID 178478191—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromophenyl)(4-chlorophenyl)methanolHCID 57659206—

Reaction Steps

4-Chlorophenylmagnesium bromide (12.97 ml, 1M solution in diethyl ether) was added slowly to a solution of 4-bromobenzaldehyde (2.0 g, 10.81 mmol) in tetrahydrofuran (25 ml) at 0° C., under an atmosphere of nitrogen. The reaction mixture was allowed to warm to room temperature and was stirred for 17 hours. Water (3 ml) was then added and the solvent was removed under reduced pressure. The residue was then partitioned between ethyl acetate and 1N HCl solution. The organic layer was washed with brine, dried (MgSO4), filtered and concentrated. The crude product was then purified by column chromatography (SiO2), eluting with ethyl acetate/petroleum ether (1:9), to yield the title compound (2.30 g). LC/MS: (PS-B3) Rt 3.49 [M−H]+297.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343953B2
Source datasetuspto-grants-2013_01
ORD IDord-6c1c0709bb2e440885abb9d48a22b1d8
Source noteuspto-grants-2013_01