HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294299Generated: November 2, 2026
Dimethylformamide → Ethyl 3-[2-ethoxy-4-[2-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]phenyl]propionate
https://huagongshe.com/reaction/1294299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(2-Chloromethylphenoxymethyl)-5-methyl-2-phenyloxazole | HCID 11099036 | — |
| Reactant | Ethyl 3-(2-ethoxy-4-hydroxyphenyl)propionate | HCID 17861342 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3-[2-ethoxy-4-[2-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]phenyl]propionate | HCID 68885449 | 93% |
Reaction Steps
A mixture of 4-(2-chloromethylphenoxymethyl)-5-methyl-2-phenyloxazole (0.50 g), ethyl 3-(2-ethoxy-4-hydroxyphenyl)propionate (0.31 g), anhydrous potassium carbonate (0.18 g) and N,N-dimethylformamide (10 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-4-[2-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]phenyl]propionate as a colorless oil (0.62 g, 93%) 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-5aa857c227384ef7a10aa4df7be10eb4 |
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| Source note | uspto-grants-2007_07 |
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