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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056961Generated: November 3, 2026

Benzyl Bromide → 3-Benzyl-5-bromo-4-methoxy-1-methyl-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/1056961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
Reactant5-Bromo-4-methoxy-1-methyl-1,3-dihydro-2H-benzimidazol-2-oneHCID 118093910—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-Benzyl-5-bromo-4-methoxy-1-methyl-1,3-dihydro-2H-benzimidazol-2-oneHCID 11809390990.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 5-bromo-4-methoxy-1-methyl-1,3-dihydro-2H-benzimidazol-2-one (60.0 mg, 0.233 mmol) in N,N-dimethylformamide (2.31 mL) was treated with cesium carbonate (380 mg, 1.17 mmol) and benzyl bromide (99.8 mg, 0.583 mmol) and stirred at 60° C. for 30 min. The reaction mixture was diluted with ethyl acetate and water. Layers were separated and the organic layer was washed with brine, dried with magnesium sulfate, filtered, and concentrated in vacuo to give the crude product. Purification by flash column chromatography (15% EtOAc/hexanes to 40% EtOAc/hexanes) gave the desired product (73 mg, 90%). LCMS calculated for C16H16BrN2O2 (M+H)+: m/z=347.1, 349.1. found: 347.0, 349.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399640B2
Source datasetuspto-grants-2016_07
ORD IDord-448b217fabbd4986a11c42e11d12f736
Source noteuspto-grants-2016_07