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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396313Generated: October 27, 2026

2-Amino-5-(trifluoromethyl)pyridine → 2-Chloroamino-5-trifluoromethylpyridine

https://huagongshe.com/reaction/2396313

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-(trifluoromethyl)pyridineHCID 735862—
Reactant2-Chloroamino-3-chloro-5-trifluoromethylpyridineHCID 18988864—
Product2-Chloroamino-5-trifluoromethylpyridineHCID 18988854—

Reaction Conditions

Temperature20 °C

Reaction Steps

Then, 16.2 g (0.1 mol) of 2-amino-5-trifluoromethylpyridine was added to the reaction product, and the mixture was heated to 20° C. and stirred at the same temperature for two hours. The reaction product was analyzed by liquid chromatography, whereby 2-chloroamino-3-chloro-5-trifluoromethylpyridine was found to have decreased to 1%, and 2-chloroamino-5-trifluoromethylpyridine was formed afresh in an amount of 31%, and 2-amino-3-chloro-5-trifluoromethylpyridine was formed in an amount of 30%. The rest was the hydrochloride of 2-amino-3-chloro-5-trimethylpyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05491239
Source datasetuspto-grants-1996_02
ORD IDord-904f24d3c6e744ce8b46d5609b8aac5f
Source noteuspto-grants-1996_02