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N,N-Dimethylaniline → 6-Methoxy-1-(2-propenyl)-2-naphthol

HRID 1582796
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1582796
C[O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([O:13][CH2:14]C=C)[CH:7]=[CH:6]2.CN(C)[C:19]1[CH:24]=CC=C[CH:20]=1>>[CH3:14][O:13][C:8]1[CH:9]=[C:10]2[C:5](=[CH:6][CH:7]=1)[C:4]([CH2:24][CH:19]=[CH2:20])=[C:3]([OH:2])[CH:12]=[CH:11]2
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 949N,N-DimethylanilineHCID 22718066HCID 22718066, Verbindung

Produkt 1

HCID 227180506-Methoxy-1-(2-propenyl)-2-naphtholAusbeute 82 %

Versuchsvorschrift

6-Methoxy-2-(2-propenyloxy)naphthalene (24.9 g, 116.2 mmol) was dissolved in N,N-dimethyl aniline (100 ml) followed by heating under reflux for 15 hours. After the organic solvent was distilled off under reduced pressure, 2N aqueous hydrochloric acid was added to the residue, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous sodium sulfate. After distilling off the solvent, the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/4), followed by recrystallization from ethyl acetate/hexane, to give 6-methoxy-1-(2-propenyl)-2-naphthol (20.3 g, Yield 82%).

Aufarbeitung

  1. temperature
by heating
  • temperatureunder reflux for 15 hours
  • distillationAfter the organic solvent was distilled off under reduced pressure, 2N aqueous hydrochloric acid
  • additionwas added to the residue, which
  • extractionwas then extracted with ethyl acetate
  • washThe organic layer was washed with saturated aqueous sodium chloride
  • dry with materialdried over anhydrous sodium sulfate
  • distillationAfter distilling off the solvent
  • customthe residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/4)
  • customfollowed by recrystallization from ethyl acetate/hexane
  • Quellen und Nachweise

    ORD-Eintrag
    ord-f92935b714294d799e6a2f4587f5c11e
    Quelldatensatz
    uspto-grants-2004_05
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US06737417B2

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