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 | Ethyl 3-(3-hydroxyphenyl)propanoate | HCID 15197885 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68884363 | HCID 68884363 | 55.5% |
Reaction Steps
A mixture of 4-(4-chloromethylphenoxymethyl)-5-methyl-2-phenyloxazole (2.42 g), ethyl 3-(3-hydroxyphenyl)propionate (1.35 g), anhydrous potassium carbonate (0.97 g) and N,N-dimethylformamide (30 mL) was stirred at 90° C. for 15 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 crystals (1.82 g, 55%) of ethyl 3-[3-[4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]phenyl]propionate from a fraction eluted with ethyl acetate-hexane (1:6, v/v). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 90-91° C.
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-7e9d7e0d84e647ec9a1343b76924810a |
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| Source note | uspto-grants-2007_07 |
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