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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984749Generated: October 29, 2026

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

https://huagongshe.com/reaction/1984749

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 numberUS07544706B2
Source datasetuspto-grants-2009_06
ORD IDord-4cb6c15064864502a6b7c201bb1e1b49
Source noteuspto-grants-2009_06