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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643227Generated: October 26, 2026

Benzamidine → 4-Dimethoxymethyl-2-phenyl-1H-imidazole

https://huagongshe.com/reaction/1643227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzamidineHCID 2332—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-1,1-dimethoxypropan-2-oneHCID 12003567—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-Dimethoxymethyl-2-phenyl-1H-imidazoleHCID 178499560—

Reaction Conditions

Temperature55 °C

Reaction Steps

To a solution of benzamidine 207 (1.44 g, 12 mmol) and potassium carbonate (4.1 g, 30 mmol) in anhydrous DMF (25 mL) is slowly added a solution of 3-bromo-1,1-dimethoxy-propan-2-one 206 (1.97 g, 10 mmol) in anhydrous DMF (10 mL) over 30 min. The mixture is then heated at 50-60° C. for 2 h. After cooling to room temperature, ethyl acetate (100 mL) and water (100 mL) were added. The organic phase is separated and the aqueous phase is extracted with ethyl acetate twice and the combined organic phase is washed with water (3×20 mL) and brine. Removal of solvents under reduced pressure and purification of the residue by column chromatography affords the desired product as a white solid. Yield: 2.08 g; LC-MS (MH+): 219. 1H NMR (300 MHz, CDCl3) δ 7.88-7.85 (m, 2H), 7.37-7.46 (m, 4H), 5.49 (s, 1H), 3.36 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119665B2
Source datasetuspto-grants-2012_02
ORD IDord-2f957bba880948e5b1c3993dc32b049e
Source noteuspto-grants-2012_02