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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935746Generated: October 25, 2026

Hydrochloric Acid → 1-benzyl-5-(1-hydroxy-4,4-diphenylbutyl)-1H-imidazole

https://huagongshe.com/reaction/1935746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1'-(3-Bromopropylidene)bisbenzeneHCID 88333—
Reactant1-Benzyl-1H-imidazole-5-carboxaldehydeHCID 2773239—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product1-benzyl-5-(1-hydroxy-4,4-diphenylbutyl)-1H-imidazoleHCID 14822290—

Reaction Steps

Magnesium turnings (0.5 g) were covered with dry tetrahydrofuran (4 ml). 1-Bromo-3,3-diphenylpropane (5.6 g) in 20 ml of dry tetrahydrofuran was added dropwise. The mixture was stirred at reflux for one hour. After being cooled to room temperature, 3-benzyl-3H-imidazole-4-carbaldehyde (3.8 g) in 20 ml of dry tetrahydrofuran was added dropwise to the Grignard reagent and the mixture was refluxed for two hours. The cooled reaction mixture was poured into a cold diluted hydrochloric acid solution. Work-up of the mixture gave the crude product, which was converted to its hydrochloride salt in ethyl acetate using dry hydrochloric acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06388090B2
Source datasetuspto-grants-2002_05
ORD IDord-1c2aeb91747747ec9fcb52c39d5ff6e5
Source noteuspto-grants-2002_05