Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 66938Erstellt: 24. Oktober 2026

p-Anisoyl chloride → 5-(4-Anisamido)-3-Trichloromethyl-1,2,4-Thiadiazole

https://huagongshe.com/de/reaction/66938

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Anisoyl chlorideHCID 7477—
Edukt3-(Trichloromethyl)-1,2,4-thiadiazol-5-amineHCID 602848—
LösungsmittelO-XyleneHCID 7237—
Produkt5-(4-Anisamido)-3-Trichloromethyl-1,2,4-ThiadiazoleHCID 13041517—

Reaktionsschritte

A solution of 11.0 g (0.05 mole) 5-amino-3-trichloromethyl-1,2,4-thiadiazole and 12.8 g (0.08 mole) 4-anisoyl chloride in 200 ml xylene was heated at reflux for 20 hours. Cooling of the reaction mixture resulted in precipitation of the crude product, which was then isolated by filtration. Purification was achieved by washing the crude product with hot hexane. Yield was 12.0 g (82%); m.p. 172° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04343945
Quelldatensatzuspto-grants-1982_08
ORD IDord-c5e879964bea48bfb1cb9bbca35b987c
Quellennotizuspto-grants-1982_08