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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424898Generated: October 27, 2026

Chlorosuccinimide → ethyl 4-chloro-5-ethyl-1H-imidazole-2-carboxylate

https://huagongshe.com/reaction/1424898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 5-ethyl-1H-imidazole-2-carboxylateHCID 14990237—
SolventChloroformHCID 6212—
Productethyl 4-chloro-5-ethyl-1H-imidazole-2-carboxylateHCID 6754984145%

Reaction Steps

NCS (3.15 g, 23.59 mmol) was added to a solution of ethyl 5-ethyl-1H-imidazole-2-carboxylate obtained in Example (1b) (3.35 g, 19.92 mmol) in chloroform (100 mL), and the mixture was stirred at room temperature for 28 hours. Saturated aqueous sodium bicarbonate solution was added to the reaction solution, followed by extraction with chloroform. Then, the organic layer was washed with brine and dried over anhydrous sodium sulfate. Following concentration under reduced pressure, the residue was purified by silica gel column chromatography (elution solvent: hexane/ethyl acetate=4/1, 3/1) to obtain 1.81 g of the title compound as a pale yellow solid (45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927588B2
Source datasetuspto-grants-2015_01
ORD IDord-8c4f36fdd026490a8b1fed8eafefe20d
Source noteuspto-grants-2015_01