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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747419Generated: October 25, 2026

Dimethylformamide → 4-(4-Chlorophenyl)-2-(2-isopropyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazole

https://huagongshe.com/reaction/747419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant1H-Imidazole, 2-(1-methylethyl)-HCID 123457—
Reactant2-Chloro-4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]oxazoleHCID 10882967—
SolventWaterHCID 962—
Product4-(4-Chlorophenyl)-2-(2-isopropyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazoleHCID 18174757—

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of 2-chloro-4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]oxazole (1.00 g), 2-isopropylimidazole (661 mg), potassium carbonate (830 mg) and N,N-dimethylformamide (10 ml) was stirred at 120-130° C. for 1 hour. The reaction mixture was poured into water (100 ml) and extracted with ethyl acetate (10 ml×2). The organic layer was dried over anhydrous magnesium sulfate and then concentrated. The residue was subjected to silica gel column chromatography, and 4-(4-chlorophenyl)-2-(2-isopropyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazole was obtained as an oil (333 mg, 28%) from an ethyl acetate-hexane (1:1, v/v)-eluted fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396848B1
Source datasetuspto-grants-2008_07
ORD IDord-ba143cf7000c4f8fa3ca98168e83ace3
Source noteuspto-grants-2008_07