Reaktion #6825
ord-66b12eb350804cde8d3d3a98c42becda
Reaktionsgleichung
hydrochloric acid
4-hydroxyphenylacetone
ammonium acetate
sodium cyanoborohydride
→
4-(2-amino-propyl)-phenol
Ausbeute 56.2%
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1SonstigeThe solvent was evaporated
- 2workup.DISSOLUTIONthe resulting residue was dissolved in water
- 3Extraktionextracted 3 times with diethyl ether
- 4workup.ADDITIONThe aqueous layer was neutralized to pH 8 by the addition of potassium hydroxide
- 5Extraktionextracted with diethyl ether
- 6TrocknenThe basic ether layer was dried over sodium sulfate
- 7Sonstigethe 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.