Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenolphthalein | HCID 4764 | — |
| Reactant | O-methylhydroxylammonium chloride | HCID 11639 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 13179942 | HCID 13179942 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 53894701 | HCID 53894701 | — |
Reaction Steps
A solution of sodium methoxide in methanol is added at room temperature, until a pink color persists, to 10.3 mg. (0.12 mmol) of o-methylhydroxylamine hydrochloride in dry MeOH containing a few crystals of phenolphthalein and 3 A molecular sieves. Methyl 2-(3-tritylamino-5-isoxazolyl)-2-ketoacetate (17.8 mg., 0.04 mmol) is then added and the reaction stirred at 65° C. for 5 hours. The sieves are removed by filtration and the filtrate concentrated to dryness under reduced pressure. After chromatography on silica gel (60-200 mesh) using 5:2 hexane:EtOAc as an eluent the title compound is isolated as a mixture of syn- and anti-methyloximes (13.7 mg., 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04394504 |
|---|
| Source dataset | uspto-grants-1983_07 |
|---|
| ORD ID | ord-8d01e5cc0a224b6d9476987494cf80df |
|---|
| Source note | uspto-grants-1983_07 |
|---|