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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345177Generated: October 25, 2026

Propylethinylcarbinol → 5-(1-Hydroxybutyl)-3-phenylisoxazole

https://huagongshe.com/reaction/345177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropylethinylcarbinolHCID 7746—
Reactant(Z)-Benzaldehyde oximeHCID 12143—
ReactantSodium HypochloriteHCID 23665760—
SolventDichloromethaneHCID 6344—
Product5-(1-Hydroxybutyl)-3-phenylisoxazoleHCID 10889347—

Reaction Steps

In 25 ml of dichloromethane, were dissolved 5.0 g (41.3 mmol) of benzaldoxime and 4.5 g (45.9 mmol) of 1-hexyne-3-ol. Under ice cooling, 29.0 g of a 12.0% aqueous solution of sodium hypochlorite were added dropwise to the solution over 30 minutes. After completion of the dropwise addition, they were reacted at 20° C. for 2 hours. After completion of the reaction, the reaction mixture was extracted with dichloromethane and the organic layer was washed with water. The organic layer was dried over anhydrous sodium sulfate and the solvent was then distilled off under reduced pressure. The residue was purified by chromatography on a silica gel column (eluent: chloroform), whereby the target compound, namely, 5-(1-hydroxybutyl)-3-phenylisooxazole was obtained as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05055585
Source datasetuspto-grants-1991_10
ORD IDord-f53c369c59d54fdfaaae38de21666242
Source noteuspto-grants-1991_10