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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169972Generated: October 28, 2026

Triethylamine → (1-Benzyl-1H-imidazol-2-yl)(2-bromo-3-methylphenyl)methanone

https://huagongshe.com/reaction/1169972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant1-BenzylimidazoleHCID 77918—
Reactant2-Bromo-3-methylbenzoic acidHCID 2735588—
SolventAcetonitrileHCID 6342—
Product(1-Benzyl-1H-imidazol-2-yl)(2-bromo-3-methylphenyl)methanoneHCID 66771155102.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 2-bromo-3-methylbenzoic acid (2.0 g, 9.3 mmol) in thionyl chloride (4.75 ml, 65.1 mmol) was heated at 65° C., under nitrogen, for 3 h. The mixture was concentrated in vacuo and to the residue was added acetonitrile (25 ml). This solution was concentrated in vacuo and the process was repeated. To the final residue was added acetonitrile (25 ml), 1-benzylimidazole (1.62 g, 10.2 mmol) and triethylamine (1.44 ml, 10.2 mmol) and the reaction mixture was heated at 60° C., under nitrogen, for 18 h. The mixture was concentrated in vacuo and to the residue was added ethyl acetate (80 ml). The solution was washed with water (40 ml) and saturated aqueous sodium hydrogen carbonate solution (40 ml), dried (MgSO4) and concentrated in vacuo to give the title compound (3.38 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825149B2
Source datasetuspto-grants-2010_11
ORD IDord-63136a82e49a469380c2285f5b6798f2
Source noteuspto-grants-2010_11