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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433577Generated: October 30, 2026

3,4-Dichlorobenzeneboronic acid → 3-(3,4-dichloro-phenyl)-5-methyl-3H-imidazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/433577

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichlorobenzeneboronic acidHCID 2734330—
ReactantHCID 178470400HCID 178470400—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
Product3-(3,4-dichloro-phenyl)-5-methyl-3H-imidazole-4-carboxylic acid ethyl esterHCID 6903870122%
Product1-(3,4-dichloro-phenyl)-5-methyl-1H-imidazole-4-carboxylic acid ethyl esterHCID 690427498%

Reaction Conditions

Temperature20 °C

Reaction Steps

A suspension of 3,4-dichlorophenylboronic acid (8.22 g, 43.1 mmol), ethyl 4-methyl-5-imidazolecarboxylate (6.64 g, 43.1 mmol) and copper(II) acetate (7.83 g, 43.1 mmol) in CH2Cl2 (86 ml) was stirred at 20° C. for 48 h. All solids were filtered, the organic phase diluted with AcOEt (500 ml) and stirred with saturated aqueous Seignette salt solution. After filtration and evaporation the residue was chromatographed (silica, eluation with gradient hexane to AcOEt) to obtain 2.8 g (22%) of 3-(3,4-dichloro-phenyl)-5-methyl-3H-imidazole-4-carboxylic acid ethyl ester [Mp. 135-136° C. (AcOEt/hexane), MS: m/e=298 (M+)] and 1.0 g (8%) of 1-(3,4-dichloro-phenyl)-5-methyl-1H-imidazole-4-carboxylic acid ethyl ester [Mp. 163-164° C. (AcOEt/hexane), MS: m/e=298 (M+)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06667335B2
Source datasetuspto-grants-2003_12
ORD IDord-a8c2fd9325dc4943851c45a2248de602
Source noteuspto-grants-2003_12