Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1C.[C:12]([Cl:16])(Cl)([Cl:14])[Cl:13]>>[N+:8]([C:6]1[CH:5]=[CH:4][C:3]([C:12]([Cl:16])([Cl:14])[Cl:13])=[C:2]([Cl:1])[CH:7]=1)([O-:10])=[O:9]Komponenten
3
Versuchsvorschrift
2-Chloro-4-nitrotoluene (2.19 g, 0.0128 mole) and dichloride monoxide (4.46 g, 0.0513 mole) in carbon tetrachloride (50 ml) were heated at 75°/18 hrs following the procedure described in Example 6. The product was dried and the solvent removed to give 1-nitro-3-chloro-4-trichloromethylbenzene (3.49 g, purity by HPLC 99.40%, yield 99.2%) as a pale yellow oil. The product was distikled in a short path still (bp 82-85/2μ) to give a pale yellow oil.
Aufarbeitung
- customThe product was dried
- customthe solvent removed
Quellen und Nachweise
- ORD-Eintrag
- ord-59e8c79b6871488db9c0e5cfc92c84a0
- Quelldatensatz
- uspto-grants-1980_10
- Patentnummer
- US04226783
Verknüpfte Notizen
Wird geladen…