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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510877Generated: November 4, 2026

2-Methylbenzimidazole → 2-Methylbenzimidazole

https://huagongshe.com/reaction/1510877

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylbenzimidazoleHCID 11984—
ReactantAmmonium ChlorideHCID 25517—
Reactant1,1,1-Trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methylpentan-2-oneHCID 10084920—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-MethylbenzimidazoleHCID 11984—
ProductHCID 10126889HCID 10126889—

Reaction Steps

To a solution of 2-methylbenzimidazole (300 mg, 2.3 mmol) in 20 mL of anhydrous THF at −30° C., n-butyl lithium (1.6 M in pentanes, 3 mL, 4.8 mmol) was slowly added. The resulting red-colored heterogeneous mixture was stirred for 2 hours at this temperature, then a solution of 1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methylpentan-2-one (700 mg, 2.55 mmol) (see Example 1) in anhydrous THF (1 mL) was added dropwise. The reaction temperature was allowed to slowly warm to room temperature over a period of 2 hours, at which time reaction was treated with saturated NH4Cl solution. The resulting mixture was extracted with diethyl ether. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo to afford an oil which was purified by chromatography on silica gel to provide 200 mg of unchanged 2-methylbenzimidazole and 60 mg of the title compound as a white solid, m.p. 80° C.-82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08212040B2
Source datasetuspto-grants-2012_07
ORD IDord-863dd95d04c44eb3b7274cccbe8b9db6
Source noteuspto-grants-2012_07