Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101718Generated: October 25, 2026

Ethyl chloroformate → Ethyl 4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxylate

https://huagongshe.com/reaction/2101718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant4-(4-Chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazoleHCID 22066083—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxylateHCID 22066075—

Reaction Steps

To a solution of 4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole (100 mg, 0.30 mmol) from Step C in THF (4 mL) cooled to −70° C. in a dry ice/acetone bath was added 1.6N n-butyl lithium in hexanes (0.22 mL, 0.36 mmol). The reaction was stirred for 1 hr and then ethyl chloroformate (0.060 mL, 60 mmol) was added via syringe. The reaction was allowed to warm to rt for 1 hr and was then quenched with aq. sodium bicarbonate and extracted twice with ethyl acetate. The organic layers were washed with brine, dried over sodium sulfate, and evaporated. The residue was purified by Prep TLC (2×1 mm, silica) (25% ethyl acetate in hexanes) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572785B2
Source datasetuspto-grants-2009_08
ORD IDord-7437d934dcff40eeaeaaa5a118334dfc
Source noteuspto-grants-2009_08