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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256398Generated: October 30, 2026

Benzimidazole, 5,6-dimethyl-2-trifluoromethyl- → HCID 15376227, compound

https://huagongshe.com/reaction/2256398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzimidazole, 5,6-dimethyl-2-trifluoromethyl-HCID 15725—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-(bromomethyl)benzoateHCID 256687—
SolventDimethylformamideHCID 6228—
ProductHCID 15376227HCID 1537622723.5%

Reaction Steps

5,6-Dimethyl-2-trifluoromethyl-1H-benzoimidazole (2.14 g, 0.01 mol) was dissolved in DMF (50 mL). Sodium hydride (60% dispersion in oil, 0.48 g, 0.012 mol) was added and the reaction mixture was stirred at ambient temperature for 0.5 hour under an atmosphere of nitrogen. 4-Bromomethyl benzoic acid methyl ester (2.29 g, 0.01 mol) was then added. The mixture was stirred at 80° C. for 18 hours. Most of the solvent was evaporated. The residue was diluted with water and extracted with ethyl acetate. The organic phase was washed with water, dried over anhydrous sodium sulfate then evaporated. The residue was crystallized from ethyl acetate/hexane twice to afford pure title compound (0.85 g, 23.5% yield) as a white solid, m.p. 150°-152° C. Anal. Calcd. for C19H17F3N2O2 : C, 62.98; H, 4.73; N, 7.73. Found: C, 62.96; H, 4.73; N, 7.56. Mass spectrum (+FAB; [M+H]+) 363. 1H-NMR (DMSO-d6 ; 400 MHz) δ 7.90 (d, 1H), 7.63 (s, 1H), 7.45 (s, 1H), 7.15 (d, 2H), 5.74 (s, 2H), 3.81 (s, 3H), 2.33 (s, 3H), and 2.30 ppm (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654436
Source datasetuspto-grants-1997_08
ORD IDord-5ae0fb11f64a4f349fa9a36f0daa11e7
Source noteuspto-grants-1997_08