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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1354413Erstellt: 24. Oktober 2026

Thionyl Chloride → N-benzylidene-4-trifluoromethylbenzenecarbohydrazonoyl chloride

https://huagongshe.com/de/reaction/1354413

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThionyl ChlorideHCID 24386—
EduktN'-benzylidene-4-trifluoromethylbenzohydrazideHCID 6736306—
LösungsmittelTolueneHCID 1140—
ProduktN-benzylidene-4-trifluoromethylbenzenecarbohydrazonoyl chlorideHCID 8659388459%

Reaktionsschritte

A mixture of N′-benzylidene-4-trifluoromethylbenzohydrazide (2.92 g), thionyl chloride (1.09 ml) and toluene (50 ml) was heated under reflux for 1 hr. After cooling, the reaction mixture was concentrated, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=8:1, volume ratio) and recrystallized from hexane to give N-benzylidene-4-trifluoromethylbenzenecarbohydrazonoyl chloride (1.85 g, yield 59%) as pale-yellow plate crystals. melting point: 95–96° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07223791B2
Quelldatensatzuspto-grants-2007_05
ORD IDord-6a103e3960444c18877c3231eeb865c1
Quellennotizuspto-grants-2007_05