Nitric Acid → HCID 21432601, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[CH:14]=[CH:13][C:5]([CH2:6][C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)=[CH:4][CH:3]=1.[N+:15]([O-])([OH:17])=[O:16].[OH-].[NH4+]>>[Cl:1][C:2]1[CH:14]=[CH:13][C:5]([CH2:6][C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=2)=[CH:4][C:3]=1[N+:15]([O-:17])=[O:16]Komponenten
4
Versuchsvorschrift
99 G. (0.487 mol) of 2-(p-chlorobenzyl)pyridine was added to 500 ml. of fuming nitric acid cooled to 10 ° while maintaining the temperature at <10° for 2 hours. The resulting mixture was poured into 800 ml. of ice, neutralized with ammonium hydroxide and allowed to stand overnight at room temperature. The resulting solid was collected, washed with water and air dried to give 2-(4-chloro-3-nitrobenzyl)pyridine as off-white prisms, m. 58°-60° C. (aq. ethanol).
Aufarbeitung
- temperaturewhile maintaining the temperature at <10° for 2 hours
- additionThe resulting mixture was poured into 800 ml
- customThe resulting solid was collected
- washwashed with water and air
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-d013ac3343f44494b03dee9870966de1
- Quelldatensatz
- uspto-grants-1977_05
- Patentnummer
- US04026936
Notizen zur Reaktion
Wird geladen…