Sodium Carbonate → Butenafine

HRID 620892

Reaktionsgleichung

Reaktionsgleichung von HRID 620892
Cl.[CH3:2][NH:3][CH2:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7][CH:6]=1.C(=O)([O-])[O-].[Na+].[Na+].[C:21]([C:25]1[CH:32]=[CH:31][C:28]([CH2:29]Br)=[CH:27][CH:26]=1)([CH3:24])([CH3:23])[CH3:22]>CN(C)C=O>[CH3:2][N:3]([CH2:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7][CH:6]=1)[CH2:29][C:28]1[CH:31]=[CH:32][C:25]([C:21]([CH3:24])([CH3:23])[CH3:22])=[CH:26][CH:27]=1

Komponenten

5

Versuchsvorschrift

N-methyl-1-naphthylmethylamine hydrochloride (2.1 g; 0.01 mole) was dissolved in 50 ml of dry dimethylformamide, and 3.71 g (0.035 mole) of anhydrous sodium carbonate was added. The mixture was stirred at room temperature, and 2.49 g (0.011 mole) of p-t-butylbenzyl bromide was added. The mixture was reacted at 30° to 40° C. for 5 hours. Ice water was added to the reaction mixture, and the mixture was extracted with toluene. The organic layer was washed with water, and toluene was evaporated. The residue was chromatographed on a silica gel column, and eluted with 5% ethyl acetate/n-hexane. The eluate was concentrated to give 2.98 g (yield 94%) of an oily substance.

Aufarbeitung

  1. customThe mixture was reacted at 30° to 40° C. for 5 hours
  2. extractionthe mixture was extracted with toluene
  3. washThe organic layer was washed with water, and toluene
  4. customwas evaporated
  5. customThe residue was chromatographed on a silica gel column
  6. washeluted with 5% ethyl acetate/n-hexane
  7. concentrationThe eluate was concentrated
  8. customto give 2.98 g (yield 94%) of an oily substance

Quellen und Nachweise

ORD-Eintrag
ord-96d668be3870437ea6a038713631e2fa
Quelldatensatz
uspto-grants-1989_04
Patentnummer
US04822822

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