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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600936Generated: October 25, 2026

(2,3-Dimethylphenyl)(1-trityl-1H-imidazol-5-yl)methanone → 1-(2,3-Dimethylphenyl)-2-phenyl-1-(1-trityl-1h-imidazol-5-yl)ethanol

https://huagongshe.com/reaction/600936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2,3-Dimethylphenyl)(1-trityl-1H-imidazol-5-yl)methanoneHCID 42631463—
ReactantHCID 178419663HCID 178419663—
SolventDichloromethaneHCID 6344—
Product1-(2,3-Dimethylphenyl)-2-phenyl-1-(1-trityl-1h-imidazol-5-yl)ethanolHCID 57437678—

Reaction Steps

A solution of (2,3-dimethylphenyl)(l-trityl-1H imidazol-5-yl)methanone (450 mg, 1.01 mmol) in dichloromethane (25 mL) at room temperature was treated with benzyl magnesium bromide (1.51 mmol) and allowed to react at room temperature and the reaction mixture was then stirred at room temperature for 5 hours. The mixture was quenched with water (10 mL) and a sat. solution of ammonium chloride (10 mL). The residue was isolated in a typical aqueous to give 1-(2,3-dimethylphenyl)-2-phenyl-1-(1-trityl-1H-imidazol-5-yl)ethanol (Intermediate 8) crude, which was taken to the next step without any purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902247B2
Source datasetuspto-grants-2011_03
ORD IDord-c655188af47c4cffae7479f12d8bed46
Source noteuspto-grants-2011_03