Benzyl Chloride → 4-Bromo-2,6-difluoro-1-(benzyloxy)benzene

HRID 579907

Reaktionsgleichung

Reaktionsgleichung von HRID 579907
[Br:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]([OH:9])=[C:4]([F:10])[CH:3]=1.[CH2:11](Cl)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(=O)([O-])[O-].[K+].[K+]>>[CH2:11]([O:9][C:5]1[C:6]([F:8])=[CH:7][C:2]([Br:1])=[CH:3][C:4]=1[F:10])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1

Komponenten

4

Edukt 3

HCID 7503Benzyl ChlorideHCID 11430Potassium CarbonateHCID 27362924-Bromo-2,6-difluorophenol

Produkt 1

HCID 142076414-Bromo-2,6-difluoro-1-(benzyloxy)benzene

Versuchsvorschrift

A stirred mixture of 4-bromo-2,6-difluorophenol (36 g, 0.172 mole), benzylchloride (21.77 g, 0.172 mole), and potassium carbonate (25 g, 0.18 mole) in demethylformamide (300 ml) was heated at 80°-90° for four hours. After cooling, the solvent was evaporated and ether added to the residue. The insoluble inorganic salts were removed by filtration, and solvent evaporated from the filtrate. The oily residue was subjected to bulb-to-bulb vacuum distillation on Kugelrohr apparatus to give the desired product as a nearly colorless oil (41 g, 80 percent): R.I.=1.5602 @ 25° C.; NMR (CDCl3) was consistent with the assigned structure.

Aufarbeitung

  1. temperaturewas heated at 80°-90° for four hours
  2. temperatureAfter cooling
  3. customthe solvent was evaporated
  4. additionether added to the residue
  5. customThe insoluble inorganic salts were removed by filtration, and solvent
  6. customevaporated from the filtrate
  7. distillationThe oily residue was subjected to bulb-to-bulb vacuum distillation on Kugelrohr apparatus

Quellen und Nachweise

ORD-Eintrag
ord-1e7166d355f54776891f441e1a93fe78
Quelldatensatz
uspto-grants-1988_06
Patentnummer
US04750931

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