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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163090Generated: October 28, 2026

Phenethyl bromide → 4-(1-phenethyl-1H-benzoimidazol-2-ylmethyl)-benzoic acid methyl ester

https://huagongshe.com/reaction/1163090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantPotassium CarbonateHCID 11430—
Reactantmethyl 4-((1H-benzo[d]imidazol-2-yl)methyl)benzoateHCID 59468704—
SolventAcetonitrileHCID 6342—
Product4-(1-phenethyl-1H-benzoimidazol-2-ylmethyl)-benzoic acid methyl esterHCID 5897078330%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of methyl 4-((1H-benzo[d]imidazol-2-yl)methyl)benzoate (200 mg, 0.75 mmol) in acetonitrile was treated with (2-bromoethyl)benzene (209 mg, 1.13 mmol) and potassium carbonate (143 mg, 0.90 mmol). The reaction mixture was heated with microwave irradiation at 100° C. for 2 h. The solvent was removed under reduced pressure and the residue was partitioned between water and dichloromethane. The organic phase was separated, dried over sodium sulfate and concentrated in vacuo. Purification of the resultant residue by flash column chromatography (silica, petroleum ether:ethyl acetate 8:2 to 1:1) afforded 4-(1-phenethyl-1H-benzoimidazol-2-ylmethyl)-benzoic acid methyl ester (30%). [M+H] 371.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820825B2
Source datasetuspto-grants-2010_10
ORD IDord-5fb8cc03dd4f43a7975b149e513880c5
Source noteuspto-grants-2010_10