Reaktion #626265

ord-3cb664679bbe4c53b79f6abc3bd5c2e2

Reaktionsgleichung

N[C@H](C(=O)O)C1CCCC1
(S)-2-amino-2-cyclopentylacetic acid
[Al+3].[H-].[H-].[H-].[H-].[Li+]
LiAlH4
N[C@H](CO)C1CCCC1
(S)-2-amino-2-cyclopentylethanol

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturheated
  2. 2
    Temperaturat reflux overnight
  3. 3
    TemperaturAfter cooling
  4. 4
    Temperaturthe reaction mixture was cooled to 0° C.
  5. 5
    Sonstigecarefully quenched by dropwise addition of water (0.4 mL)
  6. 6
    Filtrationfiltered through Celite
  7. 7
    EinengenThe filtrate was concentrated

Vorschrift

To a stirred solution of (S)-2-amino-2-cyclopentylacetic acid (1.00 g, 6.98 mmol) in THF (20 mL) was added dropwise a solution of LiAlH4 in THF (1.0 M, 10.5 mL, 10.5 mmol) at 0° C. under N2. The reaction was allowed to warm to ambient temperature and heated at reflux overnight. After cooling, the reaction mixture was cooled to 0° C. and carefully quenched by dropwise addition of water (0.4 mL) followed by 15% NaOH solution (0.4 mL) and water (1.2 mL). The mixture was stirred at ambient temperature for 15 minutes and filtered through Celite. The filtrate was concentrated to give crude (S)-2-amino-2-cyclopentylethanol, which was used in the next step without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08865726B2uspto-grants-2014_10