HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyamine hydrochloride → Ethyl 5-(4-tert-butylphenyl)-1,2-oxazole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Ethyl 4-(4-tert-butylphenyl)-2,4-dioxobutanoate | HCID 43186901 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 5-(4-tert-butylphenyl)-1,2-oxazole-3-carboxylate | HCID 20534825 | — |
Reaction Steps
Hydroxylamine hydrochloride (6.14 g, 88.0 mmol) was added to a suspension of ethyl 4-(4-tert-butylphenyl)-2,4-dioxobutanoate (20.4 g, 73.7 mmol) in absolute ethanol (300 mL) and the reaction was heated to reflux for 3 hours. After cooling to room temperature, the organics were removed in vacuo and the resulting residue was purified by silica gel chromatography, eluting with heptane to 10% methanol in dichloromethane, to obtain afford the title compound white solid was filtered, washed with water and cold ethanol and dried in vacuo to obtain ethyl 5-(4-tert-butylphenyl)isoxazole-3-carboxylate (15.9 g, 58.0 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08211927B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-5f60039cd4224f06ac7d8fa176601e6f |
| Source note | uspto-grants-2012_07 |