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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202842Generated: October 25, 2026

Acetic Anhydride → 4-(4-(trifluoromethyl)benzyloxy)pyridin-2(1H)-one

https://huagongshe.com/reaction/2202842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-(4-(Trifluoromethyl)benzyloxy)pyridine 1-oxideHCID 68657649—
Product4-(4-(trifluoromethyl)benzyloxy)pyridin-2(1H)-oneHCID 57950480—

Reaction Steps

A solution of 4-((4-(trifluoromethyl)benzyl)oxy)pyridine 1-oxide (350 mg) in acetic anhydride (6 ml) was heated under reflux for 4 h. The reaction mixture was then cooled to room temperature and concentrated in vacuo. The residue was diluted with MeOH (10 ml) and 2 M NaOH (10 ml), and heated at reflux for 1 h. The reaction mixture was cooled to room temperature and concentrated in vacuo. The residue was diluted with water and extracted with DCM. The DCM layer was concentrated in vacuo and purified by silica gel column chromatography (MeOH/DCM) to give the title compound (110 mg) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365540B2
Source datasetuspto-grants-2016_06
ORD IDord-5ade6a1d9ba7468caf5ad965a11d205c
Source noteuspto-grants-2016_06