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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543583Generated: October 25, 2026

Potassium Carbonate → N-[(+/-)-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionyl]isoxazolidine

https://huagongshe.com/reaction/543583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-(5-Trifluoromethyl-pyridin-2-yloxy)-phenolHCID 155241—
Reactant2-Chloro-1-(isoxazolidin-2-yl)propan-1-oneHCID 13314616—
SolventAcetonitrileHCID 6342—
ProductN-[(+/-)-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionyl]isoxazolidineHCID 1331462392.6%

Reaction Steps

A mixture of 4-(5-trifluoromethyl-2-pyridyloxy)phenol (25.6 g), N-[(±)-2-chloropropionyl]isoxazolidine (16.4 g) which was prepared as in Example 1, anhydrous potassium carbonate (15.2 g) and acetonitrile (300 ml) was heated under reflux with stirring for 5 hours. After cooling, the reaction mixture was filtered through a suction filter to remove solid matters and the filtrate was concentrated in vacuo. The residue was washed with the addition of water and benzene and the organic layer formed was separated and dried over anhydrous sodium sulfate. The removal of the solvent by a distillation in vacuo gave N-[(±)-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionyl]isoxazolidine (35.5 g) as a pale yellow crystalline solid. Recrystallization from a mixture of n-hexane/ethyl acetate yielded a white crystalline solid. m.p. 83°-85° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04447259
Source datasetuspto-grants-1984_05
ORD IDord-c720d9bfeb8142f68a0e1651442363a1
Source noteuspto-grants-1984_05