HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295230Generated: November 1, 2026
Water → Methyl 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolecarboxylate
https://huagongshe.com/reaction/1295230
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(Chloromethyl)-5-methyl-2-phenyl-1,3-oxazole | HCID 9794289 | — |
| Reactant | HCID 178498603 | HCID 178498603 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolecarboxylate | HCID 17861331 | 72.4% |
Reaction Steps
To a solution of methyl 3-hydroxyisoxazole-5-carboxylate (5.01 g) in N,N-dimethylformamide (70 ml) was added sodium hydride (60% in oil, 1.40 g) at 0° C. and the mixture was stirred for 15 min. Then 4-chloromethyl-5-methyl-2-phenyloxazole (7.26 g) was added and the mixture was stirred at 60° C. for 2 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 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)-5-isoxazolecarboxylate (7.96 g, yield 72%) was obtained as colorless crystals from a fraction eluted with tetrahydrofuran-hexane (1:1, volume ratio). The crystals were recrystallized from tetrahydrofuran-hexane. melting point: 123–124° C.
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-e42e971ffd8f4c3b91d94750f73c8222 |
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| Source note | uspto-grants-2007_07 |
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