Butyn-2-one → 7-(2-Fluorophenyl)-2,4-dimethyl-5,6,7,8-tetrahydroquinolin-5-one

HRID 1700515Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1700515
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]1[CH2:13][C:12](=[O:14])[CH2:11][C:10](=O)[CH2:9]1.[C:16]([O-])(=O)[CH3:17].[NH4+:20].[CH3:21][C:22](=O)[C:23]#C>C(O)CCCC>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]1[CH2:9][C:10]2[N:20]=[C:22]([CH3:23])[CH:21]=[C:16]([CH3:17])[C:11]=2[C:12](=[O:14])[CH2:13]1

Komponenten

5

Versuchsvorschrift

A mixture of 5-(2-fluorophenyl)cyclohexane-1,3-dione (1.0 g) and ammonium acetate (0.97 g) in 1-pentanol (30 ml) was refluxed for 30 minutes. To the mixture was added 3-butyn-2-one (0.97 g), and the mixture was refluxed for 14.5 hours. To the mixture was added 3-butyn-2-one (0.49 g), and the mixture was refluxed for 5 hours. Under reduced pressure, the solvent was evaporated, and the residue was dissolved in ethyl acetate. The solution was washed with water and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure, and the residue was purified with silica gel column chromatography (EtOAc/hexane) to give oil of 7-(2-fluorophenyl)-2,4-dimethyl-5,6,7,8-tetrahydroquinolin-5-one (0.12 g).

Aufarbeitung

  1. temperaturewas refluxed for 30 minutes
  2. temperaturethe mixture was refluxed for 14.5 hours
  3. temperaturethe mixture was refluxed for 5 hours
  4. customUnder reduced pressure, the solvent was evaporated
  5. dissolutionthe residue was dissolved in ethyl acetate
  6. washThe solution was washed with water and saturated brine
  7. dry with materialdried with magnesium sulfate
  8. concentrationconcentrated under reduced pressure
  9. customthe residue was purified with silica gel column chromatography (EtOAc/hexane)

Quellen und Nachweise

ORD-Eintrag
ord-dd9ce587efce4505818a057788cca13c
Quelldatensatz
uspto-grants-2002_02
Patentnummer
US06350749B1

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