Indole → 3-Naphthoylindole

HRID 55921

Reaktionsgleichung

Reaktionsgleichung von HRID 55921
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.C[Mg]Br.[C:13]1([C:23](Cl)=[O:24])[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15][CH:14]=1.[Cl-].[NH4+]>CCOCC>[C:13]1([C:23]([C:3]2[C:4]3[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=3)[NH:1][CH:2]=2)=[O:24])[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15][CH:14]=1

Komponenten

6

Versuchsvorschrift

To a cooled solution of indole (5.85 g, 50 mmol) in ether (50 ml) under nitrogen was added slowly a solution of methylmagnesium bromide (3M) in ether (17.5 ml). After addition, the reaction mixture was warmed up to room temperature and stirred for 2 h at room temperature. Then the mixture was cooled down again to 0° C., and to it was added slowly with stirring a solution of 1-naphthoylchloride (9.5 g, 50 mmol) in ether (50 ml). The resulting mixture was warmed up to room temperature and stirred for 2 h at room temperature followed by slow addition of saturated ammonium chloride solution (375 ml). The mixture was then stirred overnight at room temperature. A white solid was formed, filtered, washed by ether and dried under high vacuum to give 3-(1-naphthoyl)-1H-Indole 1 (12.3 g, 91%).

Aufarbeitung

  1. additionAfter addition
  2. temperatureThen the mixture was cooled down again to 0° C.
  3. additionto it was added slowly
  4. temperatureThe resulting mixture was warmed up to room temperature
  5. stirringstirred for 2 h at room temperature
  6. stirringThe mixture was then stirred overnight at room temperature
  7. customA white solid was formed
  8. filtrationfiltered
  9. washwashed by ether
  10. customdried under high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-8a303a3c232549e4839a627077ca7aa6
Quelldatensatz
uspto-grants-2016_09
Patentnummer
US09434687B2

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