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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968155Generated: October 29, 2026

Benzyl Bromide → 1-benzyl-1H-imidazole-2-carbaldehyde

https://huagongshe.com/reaction/1968155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant1H-imidazole-2-carbaldehydeHCID 24955—
SolventAcetonitrileHCID 6342—
Product1-benzyl-1H-imidazole-2-carbaldehydeHCID 13908296.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 1H-imidazole-2-carbaldehyde (240 mg, 2.4 mmol) and potassium carbonate (662 mg, 4.8 mmol) in acetonitrile (5 mL) at 0° C. was added dropwise (bromomethyl)benzene (493 mg, 2.88 mmol). The mixture was stirred at 40° C. for 4 hr. Then the mixture was filtrated, evaporated to remove the acetonitrile from the filtrate, added EtOAc to extract the residues, and washed the extract with brine and water. The organic layer was dried with anhydrous Na2SO4, concentrated, and chromatographed on a silica gel column (EtOAc:hexane=1:9) to obtain the title compound (430 mg, yield 95%). LC-MS (ESI) m/z: 187 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420650B2
Source datasetuspto-grants-2013_04
ORD IDord-fe0b70b956df4ae6ac3c8b39f49b4f6e
Source noteuspto-grants-2013_04