Triethylamine → HCID 131728602, Verbindung

HRID 1928987Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1928987
[CH2:1]([N:8]1[CH2:13][CH2:12][CH:11]([OH:14])[CH:10]([CH3:15])[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.[CH3:23][C:24]([CH3:29])([CH3:28])[C:25](Cl)=[O:26]>C1COCC1>[CH2:1]([N:8]1[CH2:13][CH2:12][C@@H:11]([O:14][C:25](=[O:26])[C:24]([CH3:29])([CH3:28])[CH3:23])[C@H:10]([CH3:15])[CH2:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Komponenten

5

Edukt 3

HCID 8471TriethylamineHCID 62493Pivaloyl chlorideHCID 136114921-Benzyl-3-methylpiperidin-4-ol

Produkt 1

HCID 131728602HCID 131728602, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a cis/trans mixture of 1-benzyl-3-methyl-piperidin-4-ol (50 g, 243 mmol, prepared as described in Can. J. Chem. (1972) 50, 803) in THF is added triethylamine (51 ml, 365 mmol) followed by 2,2-dimethyl-propionyl chloride (45 ml, 365 mmol). The reaction is exothermic and a precipitate is formed. The mixture is heated under reflux for 18 hours, cooled, filtered and washed with ether. The organic layers are washed with 1N-NaOH and brine, dried and evaporated. The crude is purified by chromatography on silicagel using hexane and EtOAc (5%) to give pure trans-isomer as a colourless oil.

Aufarbeitung

  1. customa precipitate is formed
  2. temperatureThe mixture is heated
  3. temperatureunder reflux for 18 hours
  4. temperaturecooled
  5. filtrationfiltered
  6. washwashed with ether
  7. washThe organic layers are washed with 1N-NaOH and brine
  8. customdried
  9. customevaporated
  10. customThe crude is purified by chromatography on silicagel
  11. customto give pure trans-isomer as a colourless oil

Quellen und Nachweise

ORD-Eintrag
ord-58911cb56efe440596df9e63e813bde2
Quelldatensatz
uspto-grants-2012_05
Patentnummer
US08183366B2

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