Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4-Chloromethylphenoxy)methyl-5-methyl-2-phenyloxazole | HCID 10946940 | — |
| Reactant | HCID 17861281 | HCID 17861281 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68886469 | HCID 68886469 | 72.6% |
Reaction Steps
A mixture of 4-(4-chloromethylphenoxymethyl)-5-methyl-2-phenyloxazole (1.44 g), ethyl 3-(2-ethoxy-5-hydroxyphenyl)propionate (1.0 g), anhydrous potassium carbonate (0.58 g) and N,N-dimethylformamide (50 mL) was stirred at 90° C. for 2 hrs. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The obtained residue was subjected to silica gel column chromatography to give ethyl 3-[2-ethoxy-5-[4-[(5-methyl-2-phenyl-4oxazolyl)methoxy]benzyloxy]phenyl]propionate as an oil (1.57 g, 72%) from a fraction eluted with ethyl acetate-hexane (1:6, v/v).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07238716B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-a927f49bebf74037a97f156fc597f35f |
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| Source note | uspto-grants-2007_07 |
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