Reaktion #4468

ord-735fc3dbd8da40b9ad499f1ee9ee5a7e

Reaktionsgleichung

ClCc1ccc2ccccc2n1
2-chloromethyl quinoline
Oc1ccccc1
phenol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
[I-].[Na+]
sodium iodide
c1ccc(OCc2ccc3ccccc3n2)cc1
desired compound
c1ccc(OCc2ccc3ccccc3n2)cc1
2-Phenoxymethyl quinoline

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas refluxed for about 4 hours
  2. 2
    Filtrationfiltered
  3. 3
    Einengenthe filtrate was concentrated
  4. 4
    workup.DISSOLUTIONdissolved in ether
  5. 5
    WaschenThe ether solution was washed thoroughly with lN NaOH solution, water and brine
  6. 6
    TrocknenAfter drying the ether solution over anhydrous magnesium sulfate
  7. 7
    Filtrationfiltering off the drying agent
  8. 8
    Sonstigethe solvent was evaporated off
  9. 9
    Sonstigeto leave the crude product which
  10. 10
    Sonstigewas crystallized from hexane and ether

Vorschrift

A mixture of 2-chloromethyl quinoline (0.05 mol), phenol (0.055 mol), finely powdered potassium carbonate (0.055 mol), cesium carbonate (0.005 mol) and sodium iodide (0.0025 mol) in acetone was refluxed for about 4 hours. The reaction mixture was cooled to room temperature and filtered and the filtrate was concentrated and dissolved in ether. The ether solution was washed thoroughly with lN NaOH solution, water and brine. After drying the ether solution over anhydrous magnesium sulfate, and filtering off the drying agent, the solvent was evaporated off to leave the crude product which was crystallized from hexane and ether to yield the desired compound as a light yellow solid, m.p. 79.5°-80.5° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04725619uspto-grants-1988_02