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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467776Generated: November 2, 2026

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

https://huagongshe.com/reaction/1467776

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 numberUS08999987B2
Source datasetuspto-grants-2015_04
ORD IDord-ba9e23e46abc401c93f6d74ed348af48
Source noteuspto-grants-2015_04