Potassium Carbonate → 8-Bromo-2,2-dimethyl-2H-1,4-benzoxazin-3(4H)-one

HRID 723313Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 723313
Br[C:2]([CH3:15])([CH3:14])[C:3]([NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([Br:12])[C:7]=1[OH:13])=[O:4].C([O-])([O-])=O.[K+].[K+].O.C(OCC)(=O)C>CN(C=O)C>[Br:12][C:8]1[C:7]2[O:13][C:2]([CH3:15])([CH3:14])[C:3](=[O:4])[NH:5][C:6]=2[CH:11]=[CH:10][CH:9]=1

Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 218735182-bromo-N-(3-bromo-2-hydroxy-phenyl)-2-methyl-propionamideHCID 22728543Water ethylacetate

Produkt 1

HCID 218735118-Bromo-2,2-dimethyl-2H-1,4-benzoxazin-3(4H)-oneAusbeute 84,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel2×

Reaktionsbedingungen

Temperatur
150 °C

Versuchsvorschrift

The 2-bromo-N-(3-bromo-2-hydroxy-phenyl)-2-methyl-propionamide of step 1 was dissolved in DMF (200 ml), and the DMF solution was added to K2CO3 (6.3 g, 45.58 mmol). The mixture was heated overnight at 150° C., then cooled and poured into a mixture of water/ethyl acetate. The organic fraction was washed with brine. After drying over MgSO4, the organic fraction was concentrated in vacuo and resulting brown residue was purified by flash chromatography to give 8-Bromo-2,2-dimethyl-4H-benzo[1,4]oxazin-3-one as a white solid (84.6%). MS: (M−H)−256.

Aufarbeitung

  1. temperaturecooled
  2. washThe organic fraction was washed with brine
  3. dry with materialAfter drying over MgSO4
  4. concentrationthe organic fraction was concentrated in vacuo
  5. customresulting brown residue
  6. customwas purified by flash chromatography

Quellen und Nachweise

ORD-Eintrag
ord-b6b6f493c77d48b48327b05f16b0e37b
Quelldatensatz
uspto-grants-2006_11
Patentnummer
US07141562B2

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