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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841209Generated: November 1, 2026

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

https://huagongshe.com/reaction/1841209

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 numberUS06683097B2
Source datasetuspto-grants-2004_01
ORD IDord-e73fd58362604b01b5a0a0a99a96bd9d
Source noteuspto-grants-2004_01