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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382513Generated: October 24, 2026

Sodium hydride → (E)-2-Styryl-1-(3-trifluoromethylpyridin-2-yl)-1H-benzimidazole

https://huagongshe.com/en/reaction/382513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-3-(trifluoromethyl)pyridineHCID 589833—
Reactant2-[(E)-2-phenylethenyl]-1H-benzimidazoleHCID 5708003—
CatalystCopperHCID 23978—
SolventDimethylacetamideHCID 31374—
Product(E)-2-Styryl-1-(3-trifluoromethylpyridin-2-yl)-1H-benzimidazoleHCID 227366475%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of (E)-2-styryl-1H-benzimidazole (0.49 g, 2.2 mmol) in dimethylacetamide (20 ml) at 0° C. under a nitrogen atmosphere was added sodium hydride (0.11 g, 2.8 mmol). After stirring at 0° C. for 20 min. and then at room temperature for 30 min., a solution of 2-chloro-3-trifluoromethylpyridine (0.60 g, 3.3 mmol) in dimethylacetamide (5 ml) was added. The resulting mixture was heated to reflux for about 3 h 20 min. After cooling, copper bronze (0.45 g, 7.1 mg-atom) was added and heating was continued for 9 h 20 min. The reaction mixture was filtered through a pad of celite and the filtrate was diluted with dichloromethane (200 ml), washed consecutively with water (3×200 ml) and brine (100 ml), dried (magnesium sulfate) and concentrated to dryness. Purification by column chromatography (silica gel, 150 g; n-hexane/ethyl acetate (2/1)) followed by recrystallization from a mixture of isopropyl ether and n-hexane yielded 37 mg (5%) of the titled compound as white solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310079B1
Source datasetuspto-grants-2001_10
ORD IDord-b84f5879348b4393850fb728e75dac59
Source noteuspto-grants-2001_10