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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101715Generated: October 31, 2026

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

https://huagongshe.com/reaction/2101715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 22066060HCID 22066060—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4,5-di-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxylateHCID 22066076—

Reaction Steps

To a solution of 4,5-di-(2,4-dichlorophenyl)-1-methylimidazole (200 mg, 0.54 mmol) from Step C in THF (5 mL) cooled to −70° C. in a dry ice/acetone bath was added 1.6N n-butyl lithium in hexanes (0.40 mL, 0.65 mmol). The reaction was stirred for 1 hr and then ethyl chloroformate (0.10 mL, 1.1 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-6f99bedacc5e4533af057db0e043aec7
Source noteuspto-grants-2009_08