Reaktion #220422

ord-37e0a932e2684d23b3114823e2c758d0

Reaktionsgleichung

[H-].[Na+]
sodium hydride
O=C1Cc2ccccc2-c2ccccc2N1
5,7-dihydro-6H-dibenz[b,d]azepin-6-one
CI
methyl iodide
CC1C(=O)Nc2ccccc2-c2ccccc21
title compound
Ausbeute 63.7%
CC1C(=O)Nc2ccccc2-c2ccccc21
7-Methyl-5,7-dihydro-6H-dibenz[b,d]azepin-6-one
Ausbeute 63.7%

Lösungsmittel

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeprepared
  2. 2
    workup.STIRRINGstirring
  3. 3
    workup.WAITcontinued for 17 h with the exclusion of light
  4. 4
    TemperaturAfter cooling
  5. 5
    Waschenwashed with NaHSO4 solution, H2O
  6. 6
    Trocknendried over Na2SO4
  7. 7
    SonstigeEvaporation and flash chromatography (SiO2, CHCl3)

Vorschrift

A round bottom flask was charged with sodium hydride (0.295 g, 7.46 mmol) in 9.0 ml of DMF and treated with 5,7-dihydro-6H-dibenz[b,d]azepin-6-one (1.3 g, 6.22 mmol) (CAS #20011-90-9, prepared as described in Brown, et. al., Tetrahedron Letters, No. 8, 667-670, (1971) and references cited therein). After stirring at 60° C. for 1 h, the solution was treated with methyl iodide (1.16 ml, 18.6 mmol) and stirring continued for 17 h with the exclusion of light. After cooling, the reaction was diluted with CH2Cl2/H2O, washed with NaHSO4 solution, H2O, and dried over Na2SO4. Evaporation and flash chromatography (SiO2, CHCl3) gave 0.885 g (63%) of the title compound as a colorless solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07390801B2uspto-grants-2008_06