Water → 4-Amino-1-(phenylmethyl)-3-pyrrolidinemethanol

HRID 1440110Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1440110
[CH2:1]([N:8]1[CH2:12][C:11](=[N:13]O)[CH:10]([C:15](OCC)=[O:16])[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].COCCO[Al+]OCCOC.[Na+].[H-].O>C1(C)C=CC=CC=1>[NH2:13][CH:11]1[CH:10]([CH2:15][OH:16])[CH2:9][N:8]([CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH2:12]1

Komponenten

5

Versuchsvorschrift

A solution of 5.24 g (0.02 mole) of 1-benzyl-3-ethoxycarbonyl-4-hydroxyiminopyrrolidine [prepared as described in step (a) above] in 10 ml of toluene was added dropwise to 28 ml of a 3.4M solution of sodium bis(2-methoxyethoxy)aluminum hydride in toluene over a period of 1 hour. The mixture was stirred at room temperature for 1.5 hours and was then heated under reflux for 2 hours. At the end of this time, the reaction mixture was allowed to cool to room temperature, after which ice and water were added to it to form a precipitate, which was removed by filtration. The filtrate was concentrated by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel using methanol as the eluent, to afford 2.16 g of 3-amino-1-benzyl-4-hydroxymethylpyrrolidine as a brown oil.

Aufarbeitung

  1. temperaturewas then heated
  2. temperatureunder reflux for 2 hours
  3. temperatureto cool to room temperature
  4. customto form a precipitate, which
  5. customwas removed by filtration
  6. concentrationThe filtrate was concentrated by evaporation under reduced pressure
  7. customthe residue was purified by column chromatography through silica gel

Quellen und Nachweise

ORD-Eintrag
ord-f068676bc58140c3b5a8a2811ab70e35
Quelldatensatz
uspto-grants-1996_03
Patentnummer
US05496951

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