Aluminium lithium hydride → 2-(Methylamino)-4-(1-naphthyloxy)-1-butanol

HRID 1834837Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1834837
[CH:1]([NH:3][CH:4]([CH2:7][CH2:8][O:9][C:10]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:13]=[CH:12][CH:11]=1)[CH2:5][OH:6])=O.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[CH3:1][NH:3][CH:4]([CH2:7][CH2:8][O:9][C:10]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:13]=[CH:12][CH:11]=1)[CH2:5][OH:6]

Komponenten

4

Edukt 2

HCID 21226445Aluminium lithium hydrideHCID 227550192-(Formylamino)-4-(1-naphthyloxy)butanol

Produkt 1

HCID 203721512-(Methylamino)-4-(1-naphthyloxy)-1-butanol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
45 °C

Versuchsvorschrift

A solution of 2-(formylamino)-4-(1-naphthyloxy)butanol (7.1 g), prepared as described in Example 3, in dry THF (150 ml) is added dropwise to a suspension of LiAlH4 (5.0 g) in THF (150 ml). The mixture is heated at 45° C for 3 hours and cooled. Excess LiAlH4 is destroyed by the careful addition of THF/water (9:1). The mixture is filtered through diatomaceous earth (Celite). The filtrate is dried and evaporated. The residue is crystallized from diethyl ether to give the title compound, γmaxCHCl3 3650, 3352, 1595 and 1580 cm-1.

Aufarbeitung

  1. temperaturecooled
  2. customExcess LiAlH4 is destroyed by the careful addition of THF/water (9:1)
  3. filtrationThe mixture is filtered through diatomaceous earth (Celite)
  4. customThe filtrate is dried
  5. customevaporated
  6. customThe residue is crystallized from diethyl ether

Quellen und Nachweise

ORD-Eintrag
ord-6c319c3bb4114440aca3b53cbbdae70b
Quelldatensatz
uspto-grants-1978_01
Patentnummer
US04071552

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