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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440338Generated: October 31, 2026

3-Phenyl-5-(1-hydroxy-2-methyl-2-butenyl)isoxazole → 3-Phenyl-5-(2-methyl-2-butenoyl)isoxazole

https://huagongshe.com/reaction/1440338

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Phenyl-5-(1-hydroxy-2-methyl-2-butenyl)isoxazoleHCID 53691029—
CatalystHCID 178418406HCID 178418406—
SolventBenzeneHCID 241—
Product3-Phenyl-5-(2-methyl-2-butenoyl)isoxazoleHCID 53950460—

Reaction Steps

Dissolved in 100 ml of benzene were 5.4 g (23.6 mmol) of 3-phenyl-5-(1 -hydroxy-2-methyl-2-butenyl)isoxazole, followed by the addition of 21.0 g (0.24 mol) of manganese dioxide. The mixture was stirred at room temperature for 24 hours. An insoluble material was filtered off and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluent: 30:1 n-hexane/ethyl acetate), whereby 3-phenyl-5- (2-methyl-2butenoyl)isoxazole was obtained as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498619
Source datasetuspto-grants-1996_03
ORD IDord-35fdcf50b1d54ae2aa2961d3d091ecc9
Source noteuspto-grants-1996_03