Water → (2 Aminoeth 1-yl) 4-naphth-1-ylpiperidine

HRID 256915

Reaktionsgleichung

Reaktionsgleichung von HRID 256915
[H-].[Al+3].[Li+].[H-].[H-].[H-].Cl.[C:8]1([CH:18]2[CH2:23][CH2:22][N:21]([CH2:24][C:25]#[N:26])[CH2:20][CH2:19]2)[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:11]=[CH:10][CH:9]=1.O.[OH-].[Na+]>O1CCCC1>[NH2:26][CH2:25][CH2:24][N:21]1[CH2:22][CH2:23][CH:18]([C:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH:11]=[CH:10][CH:9]=2)[CH2:19][CH2:20]1

Komponenten

6

Edukt 4

HCID 962Water2×HCID 14798Sodium HydroxideHCID 19784336(4 Naphth-1-ylpiperid 1-yl)acetonitrile hydrochlorideHCID 21226445Aluminium lithium hydride

Produkt 1

HCID 19096243(2 Aminoeth 1-yl) 4-naphth-1-ylpiperidine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

1.75 g of lithium aluminum hydride are added in fractions under a stream of nitrogen to a solution of 4.4 g of the compound from Example 4 in 150 ml of tetrahydrofuran. After stirring for 1 hour, the mixture is hydrolyzed with 1.75 ml of water, 3.5 ml of a 10% (wt/wt) sodium hydroxide solution and 7 ml of water. Filtration through celite, followed by evaporation of the solvent, yields an oily product which is used as it is in the following stage.

Aufarbeitung

  1. filtrationFiltration through celite
  2. customfollowed by evaporation of the solvent
  3. customyields an oily product which

Quellen und Nachweise

ORD-Eintrag
ord-281edfe014cb4076a36e46730c714a25
Quelldatensatz
uspto-grants-1993_11
Patentnummer
US05260317

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