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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877967Generated: October 25, 2026

Diethylamine → 3-[3-(2-Bromobenzyl)-3H-imidazol-4-yl]-3-methylbutan-1-ol

https://huagongshe.com/reaction/1877967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethylamineHCID 8021—
Reactant2-Bromobenzyl bromideHCID 76965—
ReactantSodium BicarbonateHCID 516892—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
Reactant4-[3-(tert-butyldimethylsilanyloxy)-1,1-dimethylpropyl]-1-trityl-1H-imidazoleHCID 53630868—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
Product3-[3-(2-Bromobenzyl)-3H-imidazol-4-yl]-3-methylbutan-1-olHCID 58827196—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-[3-(tert-butyldimethylsilanyloxy)-1,1-dimethylpropyl]-1-trityl-1H-imidazole (650 mg, 1.27 mmol) in CH3CN (10 mL) at ambient temperature is added a solution of 2-bromobenzyl bromide (420 mg, 1.68 mmol) in CH3CN (10 mL). The resulting solution is stirred at 80° C. for 6 h. The mixture is cooled to ambient temperature and diethylamine (2 mL) is added, followed by MeOH (10 mL) and the mixture is heated at 75° C. for 1 hr and stirred at ambient temperature overnight. To the reaction mixture is added HCl/dioxane (4 M, 5 mL, 20 mmol) and stirred at ambient temperature for 1 h. The mixture is neutralized with saturated aqueous NaHCO3 and concentrated. The residue is partitioned between CH2Cl2 and brine. The organic layer is washed with brine, dried over Na2SO4 and concentrated to give an oil, which is subjected to flash chromatography (silica gel) eluting with MeOH:CH2Cl2 to yield the desired compound. MS (ESI) m/z 323 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314097B2
Source datasetuspto-grants-2012_11
ORD IDord-989eb4082d89420d886d69543aab1425
Source noteuspto-grants-2012_11