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

HRID 1582796
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HRID 1582796 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 949N,N-DimethylanilineHCID 22718066HCID 22718066, 화합물

생성물 1

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

실험 절차

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%).

후처리

  1. temperatureby heating
  2. 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
  • 출처 및 근거

    ORD 기록
    ord-f92935b714294d799e6a2f4587f5c11e
    출처 데이터셋
    uspto-grants-2004_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06737417B2

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