Hydrogen Bromide → 1,2,3,4-Tetrahydroquinoxalin-5-amine
Reaktionsgleichung
Cl.Cl.[NH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([NH2:10])[C:5]=1[NH:11][CH2:12][CH2:13]O.Br>>[NH:3]1[C:4]2[CH:9]=[CH:8][CH:7]=[C:6]([NH2:10])[C:5]=2[NH:11][CH2:12][CH2:13]1Komponenten
3
Reaktionsbedingungen
- Temperatur
- -20 °C
Versuchsvorschrift
25 g (0.104 mol) of 2-[(2,6-diaminophenyl)amino]ethanol dihydrochloride are heated at 160° C. for 3 hours in 300 ml of a 62% hydrobromic acid solution. The reaction mixture is cooled to -20° C. until crystallization takes place and the precipitate obtained is dried, under nitrogen, with a mixture of methanol and ether. It is taken up in water, the pH is adjusted to alkaline with a concentrated sodium hydroxide solution and extraction is carried out with a dichloromethane/ether (50/50) mixture. Drying and evaporation are carried out.
Aufarbeitung
- customthe precipitate obtained
- dry with materialis dried, under nitrogen, with a mixture of methanol and ether
- extractionto alkaline with a concentrated sodium hydroxide solution and extraction
- customDrying
- customevaporation
Quellen und Nachweise
- ORD-Eintrag
- ord-e1702f8fc6cf4d32b294615ffdec5b23
- Quelldatensatz
- uspto-grants-1996_12
- Patentnummer
- US05589476
Notizen zur Reaktion
Wird geladen…