Reaktionsgleichung
[CH2:1]([C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([O:14]C)[N:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Br>O>[CH2:1]([C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([OH:14])[N:9]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 59 g of 2-benzyl-6-methoxypyridine and 200 ml of 47% hydrobromic acid was heated under stirring for 7 hours in an oil bath kept at 100° C. After cooling as it was, 250 ml of water was added thereto, and the resulting crystals were collected by filtration, washed with water and vacuum-dried, to give 38.9 g of the target compound.
Aufarbeitung
- temperaturewas heated
- customkept at 100° C
- temperatureAfter cooling as it
- filtrationthe resulting crystals were collected by filtration
- washwashed with water
- customvacuum-dried
Quellen und Nachweise
- ORD-Eintrag
- ord-05486037a3b44e6cb1ec2598db258d0c
- Quelldatensatz
- uspto-grants-2003_07
- Patentnummer
- US06599917B1
Verknüpfte Notizen
Wird geladen…