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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394473Generated: November 1, 2026

Sodium hydride → HCID 44430229, compound

https://huagongshe.com/reaction/1394473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-4'-nitroacetophenoneHCID 66840—
Reactant5,6-dichloro-2-(2,2,2-trifluoro-ethyl)-1H-benzimidazoleHCID 11651910—
SolventDimethylformamideHCID 6228—
ProductHCID 44430229HCID 44430229—

Reaction Steps

To 5,6-dichloro-2-(2,2,2-trifluoro-ethyl)-1H-benzimidazole (304 mg) in DMF (5 mL) was added sodium hydride (68 mg of 60% in oil dispersion). The resulting mixture was stirred at room temperature for 5 min. To the dark green solution was added 2-bromo-4′nitroacetophenone (348 mg) and the resulting mixture was stirred at room temperature overnight. The reaction mixture was quenched with water, extracted with EtOAc, and dried over Na2SO4. The crude product was purified by silica gel chromatography (10%-40% EtOAc/hexanes) to yield the title compound as an orange colored solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348438B2
Source datasetuspto-grants-2008_03
ORD IDord-9712e7595b134cfbb275ded756ba16c6
Source noteuspto-grants-2008_03