Reaktion #2439923

ord-ab1bf5a6a52040968004c284147d3180

Reaktionsgleichung

CC(=O)OCc1cccc(-c2ccccc2)n1
2-phenyl-6-(acetoxymethyl)-pyridine
OCc1cccc(-c2ccccc2)n1
2-phenyl-6-(hydroxymethyl)-pyridine
Ausbeute 81.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture was heated
  2. 2
    Temperaturat reflux temperature
  3. 3
    EinengenAfter 30 minutes the reaction mixture was concentrated with the aid of an oil pump (10 mm) at 40° C.
  4. 4
    workup.ADDITIONCH3CN was added
  5. 5
    Sonstigethe mixture was evaporated to dryness in vacuo

Vorschrift

4.5 g of 2-phenyl-6-(acetoxymethyl)-pyridine (20 mmol) was treated with an aqueous HCl solution (15%, 10 ml) and the mixture was heated at reflux temperature while stirring. After 30 minutes the reaction mixture was concentrated with the aid of an oil pump (10 mm) at 40° C., CH3CN was added, and the mixture was evaporated to dryness in vacuo and yielded 2-phenyl-6-(hydroxymethyl)-pyridine (3.0 g, 80%) as an oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE041425E1uspto-grants-2010_07