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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72325Generated: October 26, 2026

Triethylamine → 3-(4-Benzyloxy-phenyl)-isoxazole-5-carbaldehyde

https://huagongshe.com/reaction/72325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfur trioxideHCID 24682—
ReactantAmmonium ChlorideHCID 25517—
Reactant[3-(4-Benzyloxy-phenyl)-isoxazol-5-yl]-methanolHCID 64164588—
SolventDimethylsulfoxide-dichloromethaneHCID 21912085—
Product3-(4-Benzyloxy-phenyl)-isoxazole-5-carbaldehydeHCID 11818305—

Reaction Steps

[3-(4-benzyloxy-phenyl)-isoxazol-5-yl]-methanol (1.0 g, 3.5 mmol) was dissolved in 60 ml of DMSO/methylene chloride (1:2), to which solution were added dropwise sulfur trioxide.pyridine complex (1.6 g, 10.5 mmol) and triethylamine (2.44 ml, 17.5 mmol), and stirred at 0° C. for about 2 hours. The completion of the reaction was confirmed by TLC, and 10 ml of NH4Cl was added to the solution. The residual solvent was distilled under reduced pressure, and then extracted three times with water and methylene chloride. An organic layer was washed with saline solution. The obtained organic layer was distilled under reduced pressure, followed by column chromatography (ethyl acetate/Hexane=1:2) to obtain 3-(4-benzyloxy-phenyl)-isoxazol-5-carbaldehyde as a desired solid compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08828992B2
Source datasetuspto-grants-2014_09
ORD IDord-34655747a0874bf1ba2fad4898e979ab
Source noteuspto-grants-2014_09