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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875202Generated: October 30, 2026

1-Methylimidazole → (1-Methyl-1H-imidazol-2-yl)(phenyl)methanone

https://huagongshe.com/reaction/875202

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
SolventAcetonitrileHCID 6342—
Product(1-Methyl-1H-imidazol-2-yl)(phenyl)methanoneHCID 1232524092.4%

Reaction Steps

To a solution of N-methylimidazole (10.0 g, 122 mmol) in acetonitrile (120 mL) was added benzoyl chloride (14.1 mL, 122 mmol) followed by triethylamine (17.0 mL, 122 mmol), while keeping the internal temperature at 5° C. The mixture was stirred 18 h at room temperature. After filtration, the filtrate was concentrated in vacuo, diluted with ethyl acetate (200 mL) and sequentially washed with sat. aq. sodium bicarbonate (150 mL), water (100 mL) and brine (100 mL). The organic layer was dried over MgSO4 and concentrated in vacuo.to afford (1-methyl-1H-imidazol-2-yl)(phenyl)methanone [21.0 g, yield 83%; HPLC/MS: m/z=187 (M+H); log P(HCOOH)=1.38].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981111B2
Source datasetuspto-grants-2015_03
ORD IDord-0c927385c33e4ab4a660860ae4ff4a8a
Source noteuspto-grants-2015_03