HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295297Generated: November 3, 2026
Dimethylformamide → methyl 1-methyl-3-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]-1H-pyrazol-4-ylacetate
https://huagongshe.com/reaction/1295297
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Chloromethylphenoxy)methyl-5-methyl-2-phenyloxazole | HCID 10946940 | — |
| Reactant | HCID 178499559 | HCID 178499559 | — |
| Solvent | Water | HCID 962 | — |
| Product | methyl 1-methyl-3-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]-1H-pyrazol-4-ylacetate | HCID 69429917 | 59.3% |
Reaction Steps
A mixture of methyl 3-hydroxy-1-methyl-1H-pyrazol-4-ylacetate (245 mg), 4-(4-chloromethylphenoxymethyl)-5-methyl-2-phenyloxazole (452 mg), potassium carbonate (398 mg) and N,N-dimethylformamide (10 ml) was stirred at 60° C. for 6 hrs. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and methyl 1-methyl-3-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]-1H-pyrazol-4-ylacetate (382 mg, yield 59%) was obtained as a colorless oil from a fraction eluted with ethyl acetate-hexane (2:1, volume ratio).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07241785B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-ed05165f0da34b9e986f52b566620244 |
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| Source note | uspto-grants-2007_07 |
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