Potassium Carbonate → HCID 68690147, Verbindung

HRID 2245336Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2245336
[I-].C([N+]1(C)[CH2:14][CH2:13][C:12](=[O:15])[CH:11]([CH2:16][CH2:17][CH2:18][CH3:19])[CH2:10]1)C1C=CC=CC=1.[CH3:21][O:22][C:23]1[CH:24]=[C:25]([CH:27]=[C:28]([O:32][CH3:33])[C:29]=1[O:30][CH3:31])[NH2:26].C(=O)([O-])[O-].[K+].[K+]>O.C(O)C>[CH2:16]([CH:11]1[C:12](=[O:15])[CH2:13][CH2:14][N:26]([C:25]2[CH:27]=[C:28]([O:32][CH3:33])[C:29]([O:30][CH3:31])=[C:23]([O:22][CH3:21])[CH:24]=2)[CH2:10]1)[CH2:17][CH2:18][CH3:19]

Komponenten

6

Versuchsvorschrift

A slurry of 1-benzyl-3-butyl-1-methyl-4-oxo-piperidinium iodide (306 mg) in water (2 ml) was added in one portion to a refluxing solution of 3,4,5-trimethoxy aniline (929 mg) and anhydrous potassium carbonate (33 mg) in ethanol (4 ml). The dark solution was heated to reflux for three hours. Water was added and the reaction was extracted twice with DCM. The combined organic layers were dried over sodium sulfate, filtered and the solvent was evaporated to leave a dark oil, which was purified by flash chromatography (ethyl acetate/hexanes 1:1) to give the product as a colorless oil (520 mg). MS (ESI): 322.4 (MH+).

Aufarbeitung

  1. temperatureThe dark solution was heated
  2. temperatureto reflux for three hours
  3. extractionthe reaction was extracted twice with DCM
  4. dry with materialThe combined organic layers were dried over sodium sulfate
  5. filtrationfiltered
  6. customthe solvent was evaporated
  7. customto leave a dark oil, which
  8. customwas purified by flash chromatography (ethyl acetate/hexanes 1:1)

Quellen und Nachweise

ORD-Eintrag
ord-4d9791eba0f34d24ae92b2388f259968
Quelldatensatz
uspto-grants-2010_03
Patentnummer
US07683079B2

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