Phosphorus oxychloride → 2-Chloroquinolin-8-ol
Reaktionsgleichung
O[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[C:5]([OH:12])[CH:6]=[CH:7][CH:8]=2)[N:3]=1.P(Cl)(Cl)([Cl:15])=O>[NH4+].[OH-]>[Cl:15][C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[C:5]([OH:12])[CH:6]=[CH:7][CH:8]=2)[N:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 100 °C
Versuchsvorschrift
A mixture of 2,8-dihydroxyquinoline (4 g, 24.8 mmol, Fluka) and phosphorus oxychloride (20 mL, Aldrich) was stirred at 100° C. for 1 h. The clear solution was cooled to room temperature and poured slowly with stirring into a mixture of NH4OH (150 mL) and crushed ice (200 g). The white solid that precipitated was filtered, dissolved in concentrated HCl (200 mL) and stirred at 100° C. for 1 h. Neutralization of the cooled to room temperature acid solution with NH4OH afforded white precipitate, which was filtered, washed with water and dried to give the title compound as a white solid. MS (ESI, pos. ion) m/z: 180 (M+1).
Aufarbeitung
- temperatureThe clear solution was cooled to room temperature
- additionpoured slowly
- customThe white solid that precipitated
- filtrationwas filtered
- dissolutiondissolved in concentrated HCl (200 mL)
- stirringstirred at 100° C. for 1 h
- temperatureNeutralization of the cooled to room temperature acid solution with NH4OH afforded white precipitate, which
- filtrationwas filtered
- washwashed with water
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-de19be1e8d5a4ca0b95dd33164587ac9
- Quelldatensatz
- uspto-grants-2009_09
- Patentnummer
- US07582761B2
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