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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345179Generated: October 26, 2026

Hydrochloric Acid → 3-Phenyl-5-butyrylisoxazole

https://huagongshe.com/reaction/345179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
Reactant5-(1-Hydroxybutyl)-3-phenylisoxazoleHCID 10889347—
ReactantSodium HypochloriteHCID 23665760—
SolventDichloromethaneHCID 6344—
Product3-Phenyl-5-butyrylisoxazoleHCID 10130602—

Reaction Conditions

Temperature20 °C

Reaction Steps

In 12.5 ml of dichloromethane, 4.4 g (20 mmol) of 5-(1-hydroxybutyl)-3-phenylisoxazole were dissolved. While the solution was being stirred, 35.2 g (60 mmol) of a 12.7% aqueous solution of sodium hypochlorite were added dropwise to the solution. Next, a liquid mixture which had been obtained by adding 0.48 g (6.1 mmol) of pyridine to 1.0 ml of 6N hydrochloric acid) was added dropwise over 1 hour and the reaction temperature was maintained at 20° C. After completion of the reaction, the organic layer was collected and was washed successively with a 5% aqueous solution of sodium hydrogensulfite, water and 1N hydrochloric acid. The organic layer was dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The residue was then recrystallized from ethanol, whereby the target compound, namely, 5-butyryl-3-phenylisoxazole was obtained as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05055585
Source datasetuspto-grants-1991_10
ORD IDord-986bb4f03aa34f55917a406890616c22
Source noteuspto-grants-1991_10