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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 329943Erstellt: 23. Oktober 2026

Difluoromethane → 2-Difluoromethylthio-5-pyrid-2-yl-1,3,4-thiadiazole

https://huagongshe.com/de/reaction/329943

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDifluoromethaneHCID 6345—
EduktPotassium HydroxideHCID 14797—
EduktHCID 178527949HCID 178527949—
KatalysatorPotassium IodideHCID 4875—
KatalysatorTributylammonium bromideHCID 13798051—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-Difluoromethylthio-5-pyrid-2-yl-1,3,4-thiadiazoleHCID 1987048875,1%

Reaktionsschritte

A suspension of 341.5 g (l.75 mol) of 2-mercapto-5-pyrid-2-yl-1,3,4-thiadiazole in 4000 ml of dioxane is added to a solution of 230.5 g of 85% potassium hydroxide in 800 ml of water. Then 10 g of potassium iodide and 6 g of tributylammonium bromide are added to the reaction mixture and 750 g (~8.6 mol) of gaseous difluoromethane are introduced over 41/2 hours at 22°-37° C. After evaporating off the dioxane, the reaction mixture is diluted with ethyl acetate, the aqueous phase is separated and the organic solution is washed cold with 1N sodium hydroxide and water, dried over sodium sulfate and clarified with activated carbon. They ethyl acetate is removed under vacuum and the residue is crystallised from ethyl acetate/hexane, affording 321.9 g (75.1%) of the title compound with a melting point of 90°-92° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04894380
Quelldatensatzuspto-grants-1990_01
ORD IDord-9ec7e6f0f65c41ab83ae5aecb742d22c
Quellennotizuspto-grants-1990_01