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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75485Generated: October 29, 2026

Acetic Acid → ethyl 1-(4-chlorophenyl)-2-propyl-1H-imidazole-4-carboxylate

https://huagongshe.com/reaction/75485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl bromopyruvateHCID 66144—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178449876HCID 178449876—
SolventIsopropanolHCID 3776—
Productethyl 1-(4-chlorophenyl)-2-propyl-1H-imidazole-4-carboxylateHCID 5457922625%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of N-(4-chlorophenyl)butyrimidamide (compound 3, 3.5 g, 17.80 mmol), NaHCO3 (3.14 g, 37.38 mmol) in i-PrOH was added ethyl bromopyruvate (compound 4, 4.7 mL, 37.38 mmol) under N2. The reaction mixture was stirred at 85° C. for 72 hrs, then added AcOH (15 mL). After 4 hrs, the mixture was concentrated under reduced pressure. The residue was diluted with H2O, and extracted with CH2Cl2. The organic layer was washed with saturated NaHCO3 and 1N-HCl solution, then dried over anhydrous MgSO4, filtered and concentrated in vacuo. The crude product was purified by flash column chromatography (Biotage Isolera™ FLASH Purification System was used for normal phase column chromatography with EtOAc and hexane) to provide the title compound (1.28 g, 25%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835436B2
Source datasetuspto-grants-2014_09
ORD IDord-2cd7dc2d80d24989bc3361bc4bc8049d
Source noteuspto-grants-2014_09