Sulfuric Acid → 1-Diethylamino-6-(m-methoxyphenyl)heptan-3-one

HRID 1077132Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1077132
[CH2:1]([N:3]([CH2:19][CH3:20])[CH2:4][C:5]#[C:6][CH2:7][CH2:8][CH:9]([C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH3:18])[CH:12]=1)[CH3:10])[CH3:2].S(=O)(=O)(O)[OH:22]>>[CH2:19]([N:3]([CH2:1][CH3:2])[CH2:4][CH2:5][C:6](=[O:22])[CH2:7][CH2:8][CH:9]([C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([O:17][CH3:18])[CH:12]=1)[CH3:10])[CH3:20]

Komponenten

3

Versuchsvorschrift

Dissolve 1-diethylamino-6-(m-methoxyphenyl)hept-2-yne (13.6 g) in 10% aqueous sulphuric acid (40 cc) and stir with mercuric sulphate (0.69 g) for 2 hours at 70°. Filter the cooled solution, make basic with 10% aqueous sodium hydroxide and extract with ether. Wash the ethereal solution with water and brine, and dry (Na2SO4). Evaporate the solvent and distil the residue to obtain 1-diethylamino-6-(m-methoxyphenyl)heptan-3-one which has partially eliminated to 6-(m-methoxyphenyl)hept-1-en-3-one during the distillation, b.p. 145°/12 mm Hg.

Aufarbeitung

  1. filtrationFilter the cooled solution
  2. extractionextract with ether
  3. washWash the ethereal solution with water and brine
  4. dry with materialdry (Na2SO4)
  5. customEvaporate the solvent
  6. customdistil the residue

Quellen und Nachweise

ORD-Eintrag
ord-a67a1a592125445e9d9bb445aa356d33
Quelldatensatz
uspto-grants-1976_05
Patentnummer
US03959322

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