Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961693Generated: October 31, 2026

Trifluoroacetic anhydride → 2-Chloro-5-(trifluoromethyl)pyridine 1-oxide

https://huagongshe.com/reaction/1961693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantCarbamide PeroxideHCID 31294—
Reactant2-Chloro-5-(trifluoromethyl)pyridineHCID 92342—
SolventDichloromethaneHCID 6344—
Product2-Chloro-5-(trifluoromethyl)pyridine 1-oxideHCID 15448342—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Chloro-5-trifluoromethyl-pyridine (16, 10 mmol) was dissolved in CH2Cl2 (20 mL) and UHP (Urea-hydrogen peroxide addition compound, 21 mmol) was added. The mixture was cooled to 0° C., trifluoroacetic anhydride (20 mmol) was then slowly added to the reaction mixture. It was allowed to warm to room temperature and stirred until the reaction was completed judged by TLC. The reaction was quenched with aqueous Na2SO3, stirred for 4 h, washed with saturated aqueous NaHCO3, and dried over anhydrous MgSO4. Column chromatography afforded 1.8 g of compound 17 as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415357B2
Source datasetuspto-grants-2013_04
ORD IDord-e154a1ac046f460cadcb8cbf9a7dc5a3
Source noteuspto-grants-2013_04