Water → 6-bromo-3,4-dihydro-9-methoxy-2H-1,5-benzodioxepin

HRID 1057945

Reaktionsgleichung

Reaktionsgleichung von HRID 1057945
[Br:1][C:2]1[CH:8]=[CH:7][C:6]([O:9][CH3:10])=[C:4]([OH:5])[C:3]=1[OH:11].Br[CH2:13][CH2:14][CH2:15]Br.[F-].[K+].O>CN(C=O)C>[Br:1][C:2]1[C:3]2[O:11][CH2:15][CH2:14][CH2:13][O:5][C:4]=2[C:6]([O:9][CH3:10])=[CH:7][CH:8]=1

Komponenten

6

Edukt 4

HCID 962WaterHCID 80011,3-DibromopropaneHCID 522689Potassium FluorideHCID 37058743-Bromo-6-methoxybenzene-1,2-diol

Produkt 1

HCID 232723376-bromo-3,4-dihydro-9-methoxy-2H-1,5-benzodioxepin

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

3-bromo-6-methoxycatechol (31 g) was dissolved in DMF (50 ml), mixed with 1,3-dibromopropane (36 ml) and potassium fluoride (42 g), stirred for 12 hours while heating at 110° C. The resultant was allowed to stand for cooling, mixed with water, and extracted with ether. The organic layer was washed with an aqueous sodium hydroxide solution, water, and a saturated aqueous sodium chloride solution in that order, dried over manganese sulfate, and evaporated under reduced pressure for removing the solvent. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=7/1) to give Compound IIbr-a (6.7 g, 18%) as a white solid.

Aufarbeitung

  1. temperaturefor cooling
  2. extractionextracted with ether
  3. washThe organic layer was washed with an aqueous sodium hydroxide solution, water
  4. dry with materiala saturated aqueous sodium chloride solution in that order, dried over manganese sulfate
  5. customevaporated under reduced pressure
  6. customfor removing the solvent
  7. customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate=7/1)
  8. customto give Compound IIbr-a (6.7 g, 18%) as a white solid

Quellen und Nachweise

ORD-Eintrag
ord-7d65154f56be44c5b485c0d02beb4c0a
Quelldatensatz
uspto-grants-2003_02
Patentnummer
US06514996B2

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