Reaktion #2044335
ord-aa7105c9403940bc892562f70c7c4301
Reaktionsgleichung
3-cyanomethyl-l-benzhydryl azetidine
LiAlH4
hydride
→
title compound
Ausbeute 87.0%
3-aminoethyl-1-benzhydryl azetidine
Ausbeute 87.0%
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1TemperaturThe reaction mixture was refluxed for 4 h
- 2Filtrationthe gelatinous mixture was filtered
- 3Waschenthe filter cake was washed repeatedly with THF
- 4SonstigeThe solvent was evaporated
- 5workup.DISSOLUTIONthe residue was dissolved in diethyl ether
- 6Waschenwashed with brine
- 7Trocknendried with Na2SO4
- 8SonstigeEvaporation of the solvent
Vorschrift
5.7 g (21.7 mmol) of 3-cyanomethyl-l-benzhydryl azetidine was added slowly to a suspention of 2.9 g (76.0 mmol) of LiAlH4 in 80 mL of dry THF at roomtemperature. The reaction mixture was refluxed for 4 h. Excess hydride reagent was hydrolyzed by careful addition, with cooling, of NH4 Cl(aq), the gelatinous mixture was filtered and the filter cake was washed repeatedly with THF. The solvent was evaporated, the residue was dissolved in diethyl ether, washed with brine and dried with Na2SO4. Evaporation of the solvent gave 5.0 g (87%) of the title compound.