HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Thionyl Chloride → N-benzylidene-4-trifluoromethylbenzenecarbohydrazonoyl chloride
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | N'-benzylidene-4-trifluoromethylbenzohydrazide | HCID 6736306 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | N-benzylidene-4-trifluoromethylbenzenecarbohydrazonoyl chloride | HCID 86593884 | 59% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07223791B2 |
| Quelldatensatz | uspto-grants-2007_05 |
| ORD ID | ord-6a103e3960444c18877c3231eeb865c1 |
| Quellennotiz | uspto-grants-2007_05 |