Lithium amide → HCID 21330294, Verbindung

HRID 1391236

Reaktionsgleichung

Reaktionsgleichung von HRID 1391236
[CH2:1]([C:3]1([CH3:14])[CH:8]([CH3:9])[CH:7]([OH:10])[CH2:6][C:5]([CH2:12][CH3:13])([CH3:11])[NH:4]1)[CH3:2].[C:15]([C:19]1[CH:28]=[CH:27][C:22]([C:23](OC)=[O:24])=[CH:21][CH:20]=1)([CH3:18])([CH3:17])[CH3:16].[NH2-].[Li+]>CCCCCCC>[C:15]([C:19]1[CH:20]=[CH:21][C:22]([C:23]([O:10][CH:7]2[CH2:6][C:5]([CH2:12][CH3:13])([CH3:11])[NH:4][C:3]([CH2:1][CH3:2])([CH3:14])[CH:8]2[CH3:9])=[O:24])=[CH:27][CH:28]=1)([CH3:18])([CH3:16])[CH3:17]

Komponenten

5

Versuchsvorschrift

15.0 g of 2,6-diethyl-2,3,6-trimethyl-4-piperidinol (Compound 1) and 16.0 g of methyl p-t-butylbenzoate were dissolved in 500 ml of heptane. 1.5 g of lithium amide were then added to the solution and the mixture was refluxed by heating in a flask equipped with a Dean-Stark separator. 1.5 g of methanol were first removed and this was followed by 200 ml of heptane, which distilled off over a period of 3 hours. After cooling the reaction mixture, it was washed with water and dried over magnesium sulphate; the solvent was then removed by evaporation under reduced pressure. The residue was distilled under reduced pressure, giving 28.2 g of the title compound as a colourless liquid (bp 176°-178° C./0.008 mmHg).

Aufarbeitung

  1. temperaturethe mixture was refluxed
  2. temperatureby heating in a flask
  3. customequipped with a Dean-Stark separator
  4. custom1.5 g of methanol were first removed
  5. distillationdistilled off over a period of 3 hours
  6. temperatureAfter cooling the reaction mixture, it
  7. washwas washed with water
  8. dry with materialdried over magnesium sulphate
  9. customthe solvent was then removed by evaporation under reduced pressure
  10. distillationThe residue was distilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-b1322756b7e547ee99e2b1fba4888fb3
Quelldatensatz
uspto-grants-1979_02
Patentnummer
US04141883

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