Phenol → 2-Phenoxymethyl-quinoline

HRID 568483Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 568483
Cl[CH2:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]=1.[C:13]1([OH:19])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C(=O)([O-])[O-].[K+].[K+].C(=O)([O-])[O-].[Cs+].[Cs+].[I-].[Na+]>CC(C)=O>[O:19]([CH2:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:4]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

Komponenten

7

Versuchsvorschrift

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 1N 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.

Aufarbeitung

  1. temperaturewas refluxed for about 4 hours
  2. filtrationfiltered
  3. concentrationthe filtrate was concentrated
  4. dissolutiondissolved in ether
  5. washThe ether solution was washed thoroughly with 1N NaOH solution, water and brine
  6. dry with materialAfter drying the ether solution over anhydrous magnesium sulfate
  7. filtrationfiltering off the drying agent
  8. customthe solvent was evaporated off
  9. customto leave the crude product which
  10. customwas crystallized from hexane and ether

Quellen und Nachweise

ORD-Eintrag
ord-2b5a960109b8421094a4c4c7d4b97236
Quelldatensatz
uspto-grants-1988_03
Patentnummer
US04728668

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