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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395630Generated: October 25, 2026

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

https://huagongshe.com/reaction/395630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant1H-Imidazole, 2-undecyl-HCID 85582—
Reactant2-Chloro-4-(4-chlorophenyl)-5-[3-(2-methoxyphenoxy)propyl]oxazoleHCID 10959800—
SolventWaterHCID 962—
Product4-(4-Chlorophenyl)-5-[3-(2-methoxyphenoxy)propyl]-2-(2-undecyl-1-imidazolyl)oxazoleHCID 1817471913.4%

Reaction Conditions

Temperature125 °C

Reaction Steps

A mixture of 2-chloro-4-(4-chlorophenyl)-5-[3-(2-methoxyphenoxy)propyl]oxazole (500 mg), 2-undecylimidazole (500 mg), potassium carbonate (1.38 g) and N,N-dimethylformamide (10 ml) was stirred at 120-130° C. for 4 hours. The reaction mixture was poured into water (100 ml) and extracted with ethyl acetate (100 ml×2). The organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was recrystallized from diethyl ether-hexane to give 4-(4-chlorophenyl)-5-[3-(2-methoxyphenoxy)propyl]-2-(2-undecyl-1-imidazolyl)oxazole as pale yellow prisms (100 mg, 13%). Melting point 53-54° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605629B1
Source datasetuspto-grants-2003_08
ORD IDord-5e9ab1bad1c34a1182ec20ba008237c3
Source noteuspto-grants-2003_08