Thionyl Chloride → HCID 20347860, Verbindung
Reaktionsgleichung
S(Cl)([Cl:3])=O.[C:5]([C:7]1[C:8]([CH3:16])=[C:9]([CH:13]=[CH:14][CH:15]=1)[C:10](O)=[O:11])#[N:6]>>[C:5]([C:7]1[C:8]([CH3:16])=[C:9]([CH:13]=[CH:14][CH:15]=1)[C:10]([Cl:3])=[O:11])#[N:6]Komponenten
3
Versuchsvorschrift
75 cc of thionyl chloride and 30 g of 3-cyano-2-methyl-benzoic acid [prepared by process in C. R. Acad. Sci., Vol. 235(1952), p. 1660] were refluxed for 11/2 hours and after cooling, excess thionyl chloride was removed under reduced pressure. The last traces of thionyl chloride were removed by addition of benzene and distillation under reduced pressure. The residue was purified by rectification under reduced pressure to obtain 27.4 g of 3-cyano-2-methyl-benzoyl chloride in the form of colorless crystals melting at 62° C.
Aufarbeitung
- temperatureafter cooling
- customexcess thionyl chloride was removed under reduced pressure
- customThe last traces of thionyl chloride were removed by addition of benzene and distillation under reduced pressure
- customThe residue was purified by rectification under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-bea1d8e8a9cc424cbcc478e2bc6662ef
- Quelldatensatz
- uspto-grants-1980_03
- Patentnummer
- US04192890
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