Reaktion #6825

ord-66b12eb350804cde8d3d3a98c42becda

Reaktionsgleichung

Cl
hydrochloric acid
CC(=O)Cc1ccc(O)cc1
4-hydroxyphenylacetone
CC(=O)[O-].[NH4+]
ammonium acetate
[BH3-]C#N.[Na+]
sodium cyanoborohydride
CC(N)Cc1ccc(O)cc1
4-(2-amino-propyl)-phenol
Ausbeute 56.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was evaporated
  2. 2
    workup.DISSOLUTIONthe resulting residue was dissolved in water
  3. 3
    Extraktionextracted 3 times with diethyl ether
  4. 4
    workup.ADDITIONThe aqueous layer was neutralized to pH 8 by the addition of potassium hydroxide
  5. 5
    Extraktionextracted with diethyl ether
  6. 6
    TrocknenThe basic ether layer was dried over sodium sulfate
  7. 7
    Sonstigethe solvent was removed in vacuo

Vorschrift

To a solution of 4-hydroxyphenylacetone (0.5 g, Avocado, U.K.) and ammonium acetate (2.54 g, Aldrich, U.S.A.) in 10 mL methanol was added 0.17 g of sodium cyanoborohydride (Aldrich, U.S.A.). After stirring for 72 h at rt, concentrated hydrochloric acid was added dropwise until the solution reached pH 2. The solvent was evaporated and the resulting residue was dissolved in water, then extracted 3 times with diethyl ether. The aqueous layer was neutralized to pH 8 by the addition of potassium hydroxide and extracted with diethyl ether. The basic ether layer was dried over sodium sulfate and the solvent was removed in vacuo to give 0.23 g of 4-(2-amino-propyl)-phenol.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07084154B2uspto-grants-2006_08