Hydrochloric Acid → Isoquinolyl 4-methoxyphenyl ketone

HRID 2223451

Reaktionsgleichung

Reaktionsgleichung von HRID 2223451
Br[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][CH:3]=1.BrCCBr.[Mg].[C:15]1([C:25]#N)[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH:18]=[CH:17][N:16]=1.Cl.[OH-:28].[Na+]>O1CCCC1.CO>[C:15]1([C:25]([C:2]2[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][CH:3]=2)=[O:28])[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH:18]=[CH:17][N:16]=1

Komponenten

9

Edukt 6

HCID 313Hydrochloric AcidHCID 77304-BromoanisoleHCID 78391,2-DibromoethaneHCID 14798Sodium HydroxideHCID 3060571-IsoquinolinecarbonitrileHCID 5462224Magnesium

Produkt 1

HCID 693112Isoquinolyl 4-methoxyphenyl ketone

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittelHCID 8028TetrahydrofuranLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

4-Bromoanisol (15.3 ml, 122 mmol) and a catalytic amount of 1,2-dibromoethane as an initiator were added to a mixed solution of magnesium (3059 mg, 125.8 mmol) and tetrahydrofuran (20 ml) under nitrogen atmosphere, and this reaction mixture was stirred while heating under reflux for 45 minutes. The mixture was cooled to 0° C., a solution of 1-isoquinolinecarbonitrile (10.78 g, 69.9 mmol) in tetrahydrofuran (30 ml) was added dropwise thereto, and this reaction mixture was stirred at room temperature for 2 hours. The reaction mixture was cooled on ice, concentrated hydrochloric acid (24 ml) and methanol (120 ml) were added, and this mixture was heated under reflux for 1.5 hours. After cooling on ice, the mixture was adjusted to pH 8 by adding aqueous sodium hydroxide, extracted with ether, washed with saturated brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (15.87 g).

Aufarbeitung

  1. temperaturewhile heating
  2. temperatureunder reflux for 45 minutes
  3. stirringthis reaction mixture was stirred at room temperature for 2 hours
  4. additionwere added
  5. temperaturethis mixture was heated
  6. temperatureunder reflux for 1.5 hours
  7. temperatureAfter cooling on ice
  8. extractionextracted with ether
  9. washwashed with saturated brine
  10. dry with materialdried over anhydrous magnesium sulfate
  11. concentrationconcentrated under reduced pressure
  12. customThe residue was purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-c8c3c0845c9d461bbc50acd42049eceb
Quelldatensatz
uspto-grants-2008_05
Patentnummer
US07375204B2

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