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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274532Generated: October 27, 2026

Triethylamine → 1-[(Benzyloxy)methyl]imidazol-2-yl (3,4-dimethoxy-5-nitrophenyl) ketone

https://huagongshe.com/reaction/274532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-BenzyloxymethylimidazoleHCID 14795908—
Reactant3,4-Dimethoxy-5-nitrobenzoyl chlorideHCID 21928615—
SolventAcetonitrileHCID 6342—
Product1-[(Benzyloxy)methyl]imidazol-2-yl (3,4-dimethoxy-5-nitrophenyl) ketoneHCID 19000172—

Reaction Steps

A solution of 10.0 g of 1-[(benzyloxy)- methyl]imidazole in 50 ml of acetonitrile is added dropwise within 10 minutes while cooling with ice to a solution of 13.0 g of 3,4-dimethoxy-5-nitrobenzoyl chloride and 5.4 g of triethylamine in 80 ml of acetonitrile so that the temperature does not exceed 25° . The mixture is subsequently stirred for an additional 3 hours, whereupon the solvent is distilled. After treatment with water, the mixture is extracted with ethyl acetate. After two-fold washing with water, the organic phase is dried over sodium sulfate and evaporated. The resulting oil is chromatographed on 600 g of silica gel with toluene/ethyl acetate (95:5). There is obtained 1-[(benzyloxy)methyl]imidazol-2-yl (3,4-dimethoxy-5-nitrophenyl) ketone as a yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05389653
Source datasetuspto-grants-1995_02
ORD IDord-04cc483c3e344de4b3a61033c0a61542
Source noteuspto-grants-1995_02