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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410336Generated: November 3, 2026

4-Bromobenzyl bromide → 1-(4-Bromo-benzyl)-3-methyl-1,3-dihydro-benzoimidazol-2-ylideneamine

https://huagongshe.com/reaction/410336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromobenzyl bromideHCID 68527—
ReactantHCID 178481316HCID 178481316—
SolventMethyl Ethyl KetoneHCID 6569—
Product1-(4-Bromo-benzyl)-3-methyl-1,3-dihydro-benzoimidazol-2-ylideneamineHCID 5856496661%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 1-methyl-1,3-dihydro-benzoimidazol-2-ylideneamine (0.30 g, 2.04 mmol) in 2-butanone (30 ml) was added 4-bromobenzyl bromide (0.70 g, 2.81 mmol). The reaction was heated to 90° C. where it was stirred for 30 min. After this time, the resulting suspension was cooled to rt and filtered. The collected solids were partitioned between dichloromethane and a saturated solution of NaHCO3 and the mixture was stirred for 10 min. The organic layer was separated and the aqueous phase was extracted with additional dichloromethane. The organic fractions were combined, washed with H2O, dried (Na2SO4), filtered and the filtrate was concentrated under reduced pressure to give 1-(4-bromo-benzyl)-3-methyl-1,3-dihydro-benzoimidazol-2-ylideneamine as a white solid (0.39 g, 61%). HPLC-MS 316, 318 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759520B2
Source datasetuspto-grants-2014_06
ORD IDord-cbc38494ede04e8f8a597965f6860ba8
Source noteuspto-grants-2014_06