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Dibromomethane → 6-Bromo-4-methoxy-1,3-dioxaindane

HRID 1069487
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1069487
[Br:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[C:5]([OH:10])=[C:4]([OH:11])[CH:3]=1.[C:12](=O)([O-])[O-].[K+].[K+].BrCBr>CN(C)C=O>[Br:1][C:2]1[CH:3]=[C:4]([O:11][CH3:12])[C:5]2[O:10][CH2:9][O:8][C:6]=2[CH:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 3024DibromomethaneHCID 11430Potassium CarbonateHCID 109877565-Bromo-3-methoxybenzene-1,2-diol

Produkt 1

HCID 109113966-Bromo-4-methoxy-1,3-dioxaindaneAusbeute 52 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To dimethylformamide (400 mL) was added 1-bromo-3,4-dihydroxy-5-methoxybenzene (40 g, 182 mmol), potassium carbonate (75.7 g, 548 mmol), and dibromomethane (95.2 g, 548 mmol), followed by heating to reflux for 1 hour. The solvent was evaporated in vacuo, and the residue was taken up into ethyl ether, filtered, washed with saturated potassium carbonate solution, brine, 1N citric acid solution, and brine. The organic phase was dried over anhydrous magnesium sulfate and filtered through charcoal. The filtrate was concentrated in vacuo giving a crystalline precipitate which was filtered, washed with hexane, and dried in vacuo to a solid. This material was distilled at 2 mm Hg, 125° C., giving a crystalline solid, 21.7 g, 52% yield. NMR spectra and elemental analysis were consistent with the structure.

Aufarbeitung

  1. temperatureby heating
  2. temperatureto reflux for 1 hour
  3. customThe solvent was evaporated in vacuo
  4. filtrationfiltered
  5. washwashed with saturated potassium carbonate solution, brine, 1N citric acid solution, and brine
  6. dry with materialThe organic phase was dried over anhydrous magnesium sulfate
  7. filtrationfiltered through charcoal
  8. concentrationThe filtrate was concentrated in vacuo
  9. customgiving a crystalline precipitate which
  10. filtrationwas filtered
  11. washwashed with hexane
  12. customdried in vacuo to a solid
  13. distillationThis material was distilled at 2 mm Hg, 125° C.
  14. customgiving a crystalline solid, 21.7 g, 52% yield

Quellen und Nachweise

ORD-Eintrag
ord-33add3b8bb9444f4bc4bd705b53c3c86
Quelldatensatz
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06252070B1

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