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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074065Generated: October 30, 2026

Triethylamine → ethyl 1-benzyl-1H-imidazole-2-carboxylate

https://huagongshe.com/reaction/2074065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant1-BenzylimidazoleHCID 77918—
SolventAcetonitrileHCID 6342—
Productethyl 1-benzyl-1H-imidazole-2-carboxylateHCID 39869052—

Reaction Conditions

Temperature-20 °C

Reaction Steps

148 g (936 mmol) of 1-benzyl-1H-imidazole are suspended in 480 ml of acetonitrile and, at −20° C., 120 ml (87.1 g; 860 mmol) of triethylamine are added. Over a period of 15 minutes, 211.2 ml (239 g; 2208 mmol) of ethyl chloroformate are then added dropwise. The reaction mixture is stirred at −20° C. for 10 minutes. After warming to 15 to 20° C., the reaction mixture is stirred for 18 h and then concentrated in vacuo. Water, a saturated sodium chloride solution and a saturated sodium bicarbonate solution are added to the residue, and the mixture is extracted three times with ethyl acetate. The combined organic phases are washed with a saturated sodium chloride solution and, after drying with magnesium sulfate, concentrated in vacuo. The residue is subjected to a fractional distillation under high vacuum (boiling point=173 to 181° C., pressure=1.7 to 1.2 mbar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919489B2
Source datasetuspto-grants-2011_04
ORD IDord-271f70d6d38b412b852fdbb898c72a35
Source noteuspto-grants-2011_04