HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254458Generated: October 31, 2026
Potassium Carbonate → 5-(5-Oxazolyl)-2-furanmethanol
https://huagongshe.com/reaction/2254458
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tosylmethyl isocyanide | HCID 161915 | — |
| Reactant | 5-(Hydroxymethyl)furfural | HCID 237332 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(5-Oxazolyl)-2-furanmethanol | HCID 19744686 | 66.2% |
Reaction Steps
300 mg of 5-formylfurfuryl alcohol see Japanese Laid-Open Patent Publication No. 154758/1979 was dissolved in 10 ml of methanol, and 502 mg of p-toluenesulfonylmethyl isocyanide and 329 mg of potassium carbonate were added. The mixture was heated under reflux for 1 hour. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in a mixture of water and ethyl acetate. The organic layer was separated, and dried over anhydrous magnesium sulfate. The desiccant was separated by filtration, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography Wakogel C-200, 45 g; eluting solvent: hexane/ethyl acetate=3/2→1/1] to give 260 mg (yield 66%) of the captioned compound as a pale yellow crystalline powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05234946 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-a35c3c14f4af44af9f950a744a8ed223 |
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| Source note | uspto-grants-1993_08 |
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