HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2795Generated: October 26, 2026
Sodium Chloride → 3-Furyl 4-Methyl-5-oxazolyl Ketone
https://huagongshe.com/reaction/2795
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 3-Bromofuran | HCID 89164 | — |
| Reactant | N-Methoxy-N,4-dimethyloxazole-5-carboxamide | HCID 18925369 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Furyl 4-Methyl-5-oxazolyl Ketone | HCID 18936307 | — |
Reaction Steps
3-Bromofuran (2.5 g) in dry diethylether was stirred and cooled to -70° C. under an atmosphere of dry nitrogen and n-butyllithium (2.5M solution in hexane, 6.8 ml) was added dropwise. After 30 minutes, N-methoxy-N-methyl-4-methyl-5-oxazolecarboxamide (2.89 g) in dry diethylether was added dropwise. After a further 30 minutes the mixture was allowed to warm to room temperature. Ethanol (5 ml) was added followed by saturated aqueous sodium chloride. The mixture was extracted with dichloromethane and the material thus obtained was purified by flash chromatography to give the title compound. M.p. 82°-83.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05731335 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-69d90fe1ebe346e2ad0d74e44a53c346 |
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| Source note | uspto-grants-1998_03 |
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