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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843117Generated: November 3, 2026

4-(Trifluoromethyl)pyridine → 1-Amino-4-trifluoromethylpyridinium 2,4,6-trimethylbenzenesulfonate

https://huagongshe.com/reaction/1843117

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)pyridineHCID 138055—
ReactantO-(2,4,6-Trimethylbenzenesulfonyl)hydroxylamineHCID 11830845—
SolventDichloromethaneHCID 6344—
Product1-Amino-4-trifluoromethylpyridinium 2,4,6-trimethylbenzenesulfonateHCID 86671366—

Reaction Steps

To a solution of 4-trifluoromethylpyridine (2.23 g, 15.2 mmol) in CH2Cl2 (66 mL) at 0° C., O-(mesitylsulfonyl)hydroxylamine (3.27 g, 15.2 mmol) was added. The reaction mixture was stirred at room temperature for 18 h. The reaction mixture was filtered to afford the desired product with quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946257B2
Source datasetuspto-grants-2015_02
ORD IDord-19cbd1eae1d948a99e78af11fe066759
Source noteuspto-grants-2015_02