Pyridine → HCID 22281167, Verbindung
Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH:7][S:8]([OH:11])(=[O:10])=[O:9].[C:12](OC(=O)C)(=[O:14])[CH3:13]>>[NH+:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:12]([O:9][S:8](=[O:11])(=[O:7])[O-:10])(=[O:14])[CH3:13]Komponenten
4
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
A mixture of 30 ml of acetic anhydride and 8.05 ml (0.1 mole) of pyridine is cooled to 0° C., and 5.4 ml of conc. H2SO4 is added dropwise at 0° C. under stirring. After 10 minutes, the crystals are filtered, washed with diethyl ether and dried under vacuum over P2O5 and KOH. Yield: 18.4 g (84%). IR: 1050 cm-1 sharp band, characteristic for sulfates and sulfate esters. Decomposes above 75° C., very hygroscopic. MW: 219.2 (C7H9O5NS).
Aufarbeitung
- filtrationthe crystals are filtered
- washwashed with diethyl ether
- dry with materialdried under vacuum over P2O5 and KOH
- customDecomposes above 75° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-31ef5b543ae04d0ca0c0e4bf5fa1b410
- Quelldatensatz
- uspto-grants-1984_12
- Patentnummer
- US04490364
Notizen zur Reaktion
Wird geladen…