Methanesulfonic Acid → 3-Ethylaniline mesylate
Reaktionsgleichung
[CH2:1]([C:3]1[CH:4]=[C:5]([CH:7]=[CH:8][CH:9]=1)[NH2:6])[CH3:2].[CH3:10][S:11]([OH:14])(=[O:13])=[O:12]>CO>[S:11]([OH:14])(=[O:13])(=[O:12])[CH3:10].[CH2:1]([C:3]1[CH:4]=[C:5]([CH:7]=[CH:8][CH:9]=1)[NH2:6])[CH3:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 25 °C
Versuchsvorschrift
To a solution of 3-ethylaniline (Aldrich, 4.84 g, 40 mmol) in methanol (10 mL) was added methanesulfonic acid (4.4 g, 45 mmol) at 4° C., then the reaction mixture was stirred at 25° C. for 30 minutes to yield a solution with white precipitates. The precipitates were collected by filtration, washed with ether, and dried under vacuum to afford 7.7 g of 3-ethylaniline mesylate (7.7 g, 91% yield).
Aufarbeitung
- customto yield a solution with white precipitates
- filtrationThe precipitates were collected by filtration
- washwashed with ether
- customdried under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-5f127b59b8db46b4b49d1501b882be52
- Quelldatensatz
- uspto-grants-2000_12
- Patentnummer
- US06156741
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