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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12306Erstellt: 25. Oktober 2026

Iodine → 2-Iodo-6-(trifluoromethyl)pyridin-3-amine

https://huagongshe.com/reaction/12306

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
Edukt5-Amino-2-(trifluoromethyl)pyridineHCID 2737744—
KatalysatorHCID 178418844HCID 178418844—
LösungsmittelEthanolHCID 702—
Produkt2-Iodo-6-(trifluoromethyl)pyridin-3-amineHCID 5342547996%

Reaktionsschritte

3.85 g (12.3 mM) of silver sulfate are added, with stirring and at room temperature, to a solution of 2 g (12.3 mM) of 5-amino-2-(trifluoromethyl)pyridine in 100 ml of ethanol. 3.13 g of iodine are then added and the reaction mixture is stirred at room temperature for 24 hours. The solid in suspension in the medium is removed by filtration and the filtrate is concentrated under reduced pressure. The evaporation residue is taken up in 200 ml of dichloromethane and washed with 5% sodium hydroxide solution, and then with water and dried over magnesium sulfate. The solution obtained is concentrated under reduced pressure and 3.42 g of the expected compound are thus obtained in the form of a pink solid (yield=96%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728002B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-d8ab2f2da6704ce983b0aa772fa77a07
Quellennotizuspto-grants-2010_06