Reaktionsgleichung
[Br:1][CH2:2][C:3]([CH:5]1[CH2:10][CH2:9][O:8][CH2:7][CH2:6]1)=[O:4].[N:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[CH3:17]>CO>[Br-:1].[CH3:17][C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][N+:11]=1[CH2:2][C:3](=[O:4])[CH:5]1[CH2:10][CH2:9][O:8][CH2:7][CH2:6]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 2-bromo-1-(tetrahydro-pyran-4-yl)-ethanone (0.6 g, 2.89 mmol) and 2-picoline (0.4 mL, 4.3 mmol) in methanol (10 mL) was heated to reflux and maintained overnight. The solvent was removed in vacuo to give a residue which was washed with 20% ethyl acetate in hexane to afford 2-methyl-1-[2-oxo-2-(tetrahydro-pyran-4-yl)-ethyl]-pyridinium bromide (0.75 g, 86%) as a semi-solid.
Aufarbeitung
- temperaturewas heated
- temperatureto reflux
- temperaturemaintained overnight
- customThe solvent was removed in vacuo
- customto give a residue which
- washwas washed with 20% ethyl acetate in hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-203bea987b4746448a898a969cf61fa0
- Quelldatensatz
- uspto-grants-2013_09
- Patentnummer
- US08524705B2
Verknüpfte Notizen
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