Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072198Generated: November 2, 2026

3-phenyl-5-(4-methyl-beta-hydroxyphenethyl)-N-methyl-isoxazole-4-carboxamide → N-methyl-5-(4-methylphenacyl)-3-phenyl-4-isoxazole carboxamide

https://huagongshe.com/reaction/2072198

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-phenyl-5-(4-methyl-beta-hydroxyphenethyl)-N-methyl-isoxazole-4-carboxamideHCID 20305057—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
ProductN-methyl-5-(4-methylphenacyl)-3-phenyl-4-isoxazole carboxamideHCID 20305048—

Reaction Steps

A mixture of 41.4 g. (0.123 mole) of 3-phenyl-5-(4-methyl-β-hydroxyphenethyl)-N-methyl-isoxazole-4-carboxamide and 800 ml. of acetone is treated dropwise with the addition of 92.5 ml. (0.185 mole) of Jones reagent [100 g. chromium trioxide, 160 ml. concentrated sulfuric acid with water to 500 ml.] and the resulting mixture is stirred at room temperature for 2 hours. The supernatant liquid is decanted and the solvent removed in vacuo, the residue is taken up in water/methylene chloride and the layers separated. The organic phase is washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and evaporated in vacuo. The residue is treated with ether to give a solid and then triturated with ethanol to give N-methyl-5-(4-methylphenacyl)-3-phenyl-4-isoxazole carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04049813
Source datasetuspto-grants-1977_09
ORD IDord-a132dabc8a8f4c59a9a79faabb02a20e
Source noteuspto-grants-1977_09