HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716856Generated: November 2, 2026
Potassium Carbonate → Ethyl 2-[4-(hydroxymethyl)phenyl]-1,3-oxazole-4-carboxylate
https://huagongshe.com/reaction/1716856
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Hydroxymethyl)benzeneboronic acid | HCID 2734706 | — |
| Reactant | Ethyl 2-chlorooxazole-4-carboxylate | HCID 2763184 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 2-[4-(hydroxymethyl)phenyl]-1,3-oxazole-4-carboxylate | HCID 46834789 | 70% |
Reaction Steps
A solution of ethyl 2-chloro-1,3-oxazole-4-carboxylate (0.59 g, 3.36 mmol) in dioxane was treated with 4-(hydroxymethyl)phenyl boronic acid (0.766 g, 5.04 mmol), K2CO3 (0.929 g, 6.72 mmol), t-Bu3PhBF4 (0.049 g, 0.168 mmol) heated to 80° C. then treated with Pd2(dba)3 (0.154 g 0.168 mmol) and stirred overnight at 90° C. The reaction mixture was diluted with EtOAc, washed with water, saturated sodium chloride, dried over MgSO4 and concentrated in in vacuo. The resultant residue was purified by flash chromatography (silica, EtOAc:hexanes 20→50%) to give the title product in 70% yield, identified by NMR and mass spectral analyses. LCMS (ESI+) 248 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803825B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-5480ed18099c49f081b718c2ece56031 |
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| Source note | uspto-grants-2010_09 |
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