Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386618Generated: November 2, 2026

Hydroxyamine hydrochloride → Methyl 4-{3-[4-(pentyloxy)phenyl]-1,2-oxazol-5-YL}benzoate

https://huagongshe.com/reaction/1386618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant1-(4-Methoxycarbonylphenyl)-3-(4-n-pentyloxyphenyl)-1-propene-3-oneHCID 54178372—
CatalystHCID 178418406HCID 178418406—
Solvent1,2-DichloroethaneHCID 11—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-{3-[4-(pentyloxy)phenyl]-1,2-oxazol-5-YL}benzoateHCID 2118249923.6%

Reaction Steps

A solution of 1-(4-Methoxycarbonylphenyl)-3-(4-n-pentyloxyphenyl)-1-propen-3-one (4.0 g) and hydroxyamine hydrochloride (3.93 g) in ethanol (40 ml) was refluxed for 4 hours. The mixture was diluted with ethyl acetate, and the organic layer was washed with water (×2), brine and dried over magnesium sulfate. The solvents were removed under reduced pressure to give crude oxime. To a solution of crude oxime in 1,2-dichloroethane (20 ml) was added activated-manganese(IV) oxide (10.0 g). The reaction mixture was refluxed for 2 hours and filtered. The residue was washed with dichloromethane. The solvents were removed under reduced pressure and the residue was triturated with acetonitrile. The solid was collected by filtration and dried to give Methyl 4-[3-(4-n-pentyloxyphenyl)isoxazol-5-yl]benzoate (0.98 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265536B1
Source datasetuspto-grants-2001_07
ORD IDord-46ccb1d39d8547b9b724a41c8a6ec8b7
Source noteuspto-grants-2001_07