Reaktion #540285

ord-601a0271a430444ca570020d1a338b7c

Reaktionsgleichung

N#Cc1ccc(OCc2ccccc2)cc1
4-benzyloxybenzonitrile
[K+].[OH-]
KOH
NC(=O)c1ccc(OCc2ccccc2)cc1
product
Ausbeute 101.3%
NC(=O)c1ccc(OCc2ccccc2)cc1
4-Benzyloxybenzamide
Ausbeute 101.3%

Reagenzien

Keine

Lösungsmittel

Reaktionsbedingungen

Temperatur
78°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe resulting reaction mixture
  2. 2
    SonstigeAfter the completion of the reaction (TLC monitoring)
  3. 3
    Extraktionextracted with ethyl acetate (3×50 ml)
  4. 4
    TrocknenThe combined organic layer was dried over Na2SO4
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated under vacuum

Vorschrift

To a solution of 4-benzyloxybenzonitrile (0.61 g, 2.91 mmol) in 15 ml of tert-butanol was added fine powder of KOH (1.22 g, 21.78 mmol) and the resulting reaction mixture was refluxed for 4 h at 78° C. After the completion of the reaction (TLC monitoring), added brine solution and extracted with ethyl acetate (3×50 ml). The combined organic layer was dried over Na2SO4, filtered and concentrated under vacuum, to get the product (0.67 g) that was used as such for the next step.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08492414B2uspto-grants-2013_07