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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72313Generated: October 24, 2026

Propargyl alcohol → [3-(4-Benzyloxy-phenyl)-isoxazol-5-yl]-methanol

https://huagongshe.com/en/reaction/72313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
Reactant4-Benzyloxy-benzaldehyde oximeHCID 763359—
ReactantSodium HypochloriteHCID 23665760—
SolventDichloromethaneHCID 6344—
Product[3-(4-Benzyloxy-phenyl)-isoxazol-5-yl]-methanolHCID 64164588—

Reaction Steps

4-benzyloxy-benzaldehyde oxime (2.27 g, 10 mmol-a compound of 92% purity) was dissolved in methylene chloride (40 ml, 0.25 M), to which solution was added propargyl alcohol (1.77 ml, 30 mmol). To the resulting solution was very slowly dropwise added 10% NaOCl (13.7 ml, 20 mmol) at 0° C., using a dropping funnel. After the addition of NaOCl was completed, the mixture was stirred for about 5 hours while increasing the temperature slowly to room temperature. The completion of the reaction was confirmed by liquid chromatography, and the mixture was distilled under reduced pressure to remove the methylene chloride. Water (200 ml) was added to the residue and the resulting solid was filtered off. The filtered compound was washed with excess of water and finally washed with diethyl ether. The thus-obtained solid compound was recrystallized from ethyl acetate/hexane (1:2) to obtain 2.50 g of [3-(4-benzyloxy-phenyl)-isoxazol-5-yl]-methanol as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828992B2
Source datasetuspto-grants-2014_09
ORD IDord-5fbbabaf954345bd939643f966166217
Source noteuspto-grants-2014_09