HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395618Generated: October 25, 2026
Dimethylformamide → 4-(4-Chlorophenyl)-2-(2-ethyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazole
https://huagongshe.com/reaction/395618
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Ethylimidazole | HCID 66130 | — |
| Reactant | 2-Chloro-4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]oxazole | HCID 10882967 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Chlorophenyl)-2-(2-ethyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazole | HCID 18174686 | 38% |
Reaction Steps
A mixture of 2-chloro-4-(4-chlorophenyl)-5-[3-(2-methylphenoxy)propyl]oxazole (1.00 g), 2-ethylimidazole (960 mg), potassium carbonate (1.38 g) 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 the solid precipitate was filtered, air-dried and recrystallized from acetone-isopropyl ether to give 4-(4-chlorophenyl)-2-(2-ethyl-1-imidazolyl)-5-[3-(2-methylphenoxy)propyl]oxazole as pale yellow prisms (438 mg, 38%). Melting point 91-92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06605629B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-45ac57ca6cbb4eb1913bf30e3a6ba038 |
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| Source note | uspto-grants-2003_08 |
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