HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395629Generated: October 29, 2026
Dimethylformamide → 4-(4-Chlorophenyl)-5-[3-(2-methoxyphenoxy)propyl]-2-(2-propyl-1-imidazolyl)oxazole
https://huagongshe.com/reaction/395629
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Propylimidazole | HCID 162617 | — |
| Reactant | 2-Chloro-4-(4-chlorophenyl)-5-[3-(2-methoxyphenoxy)propyl]oxazole | HCID 10959800 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Chlorophenyl)-5-[3-(2-methoxyphenoxy)propyl]-2-(2-propyl-1-imidazolyl)oxazole | HCID 11826511 | 39% |
Reaction Steps
A mixture of 2-chloro-4-(4-chlorophenyl)-5-[3-(2-methoxyphenoxy)propyl]oxazole (500 mg), 2-propylimidazole (1.10 g), 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), the resulting solid precipitate was filtered, air-dried and recrystallized from acetone-hexane to give 4-(4-chlorophenyl)-5-[3-(2-methoxyphenoxy)propyl]-2-(2-propyl-1-imidazolyl)oxazole as pale yellow prisms (233 mg, 39%). Melting point 89-90° 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-1db3d316126946e99dc1318123703cab |
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| Source note | uspto-grants-2003_08 |
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