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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181315Generated: October 26, 2026

Potassium Carbonate → Ethyl 2-[4-(2-bromo-5-chlorobenzyloxy)phenyl]-1-cyclohexylbenzimidazole-5-carboxylate

https://huagongshe.com/reaction/1181315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-5-chlorotolueneHCID 84476—
Reactant2-Bromo-5-chlorobenzyl bromideHCID 11846505—
ReactantEthyl 1-cyclohexyl-2-(4-hydroxyphenyl)benzimidazole-5-carboxylateHCID 135486203—
SolventDimethylformamideHCID 6228—
SolventWater ethylacetateHCID 22728543—
ProductEthyl 2-[4-(2-bromo-5-chlorobenzyloxy)phenyl]-1-cyclohexylbenzimidazole-5-carboxylateHCID 1020997764%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Bromo-5-chlorobenzyl bromide prepared from 2-bromo-5-chlorotoluene (50 g), N-bromosuccinimide and N,N′-azobisisobutyronitrile, and ethyl 1-cyclohexyl-2-(4-hydroxyphenyl)benzimidazole-5-carboxylate (50 g) obtained in Example 3 were suspended in dimethylformamide (300 ml). Potassium carbonate (38 g) was added and the mixture was stirred for 1 hr at 80° C. with heating. The reaction mixture was allowed to cool and then added to a mixed solvent of water-ethyl acetate. The precipitated crystals were collected by filtration to give the title compound (50 g, yield 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285551B2
Source datasetuspto-grants-2007_10
ORD IDord-99619a02d4e340f7ae9af021629e18bd
Source noteuspto-grants-2007_10