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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422502Generated: October 30, 2026

Ethyl chloroformate → ethyl 4-iodo-2-methyl-1H-imidazole-1-carboxylate

https://huagongshe.com/reaction/422502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178433060HCID 178433060—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
Productethyl 4-iodo-2-methyl-1H-imidazole-1-carboxylateHCID 6659832195.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-iodo-2-methyl-1H-imidazole (162 mg, 0.78 mmol) in THF (2.6 mL, 0.3M) containing DIEA (0.33 mL, 1.95 mmol) and DMAP (47 mg, 0.039 mmol), cooled in a ice bath at 0° C., was added a solution of Ethyl chloroformate (211 mg, 1.95 mmol) in THF (2 mL, 1M). The reaction mixture was heated at 50° C. for 48 h and then concentrated. The residue was dissolved in DCM and the organic layer was washed with saturated NaCl, dried over magnesium sulfate, filtered and evaporated. The crude product was purified by flash chromatography (Prepacked column 10 g, DCM/MeOH: 97/3 as eluent) to afford 208 mg of ethyl 4-iodo-2-methyl-1H-imidazole-1-carboxylate (95%) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101637B2
Source datasetuspto-grants-2012_01
ORD IDord-cc1cddb27d43467bb0083b1f759e163c
Source noteuspto-grants-2012_01