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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 66939Erstellt: 24. Oktober 2026

Benzoyl chloride, 3-nitro- → 5-(3-Nitrobenzamido)-3-Trichloromethyl-1,2,4-Thiadiazole

https://huagongshe.com/de/reaction/66939

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chloride, 3-nitro-HCID 8495—
Edukt3-(Trichloromethyl)-1,2,4-thiadiazol-5-amineHCID 602848—
LösungsmittelO-XyleneHCID 7237—
Produkt5-(3-Nitrobenzamido)-3-Trichloromethyl-1,2,4-ThiadiazoleHCID 1304151869,1%

Reaktionsschritte

A solution of 21.8 g (0.1 mole) 5-amino-3-trichloromethyl-1,2,4-thiadiazole and 18.6 g (0.1 mole) 3-nitrobenzoyl chloride in 250 ml xylene was heated at reflux for 20 hours. Unreacted starting amino compound was recovered by cooling the reaction mixture and filtering the resulting precipitate. The filtrate was concentrated in vacuo and the residue recrystallized from xylene. After washing with petroleum ether, 25.4 g (69% yield) of pure product was obtained; m.p. 198° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04343945
Quelldatensatzuspto-grants-1982_08
ORD IDord-de6e7a9e35cd4ea48025e0a704ebed64
Quellennotizuspto-grants-1982_08