HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 5-ethoxy-4,5-dihydro-1,2-oxazole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | HCID 54377377 | HCID 54377377 | — |
| Product | Ethyl 5-ethoxy-4,5-dihydro-1,2-oxazole-3-carboxylate | HCID 14811462 | 76% |
Reaction Steps
17.22 g of 4-ethoxy-2-oxo-3-butenoic acid prepared according to the method of L. Tietze et al. (Lutz-F. Tietze, Heinrich Meier and Edgar Voss, Synthesis 1988, 274) are dissolved in 50 ml of anhydrous ethanol, and 7.34 g of hydroxylamine hydrochloride is added thereto, and the mixture is stirred at room temperature for 4 hours. The reaction mixture is added with water and extracted with methylene chloride. The organic layer is washed with water, dried, and evaporated. The resulting residue is distilled under reduced pressure to yield 14.3 g of ethyl 5-ethoxyisoxazoline-3carboxylate. (yield 76%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05760244 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-350bf05947a1475191c1e6e7416faf16 |
| Source note | uspto-grants-1998_06 |