Dimethyl Sulfate → 2-Bromo-4-chloroanisole

HRID 52621

Reaktionsgleichung

Reaktionsgleichung von HRID 52621
[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[OH:9].[C:10](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O>CC(C)=O>[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[O:9][CH3:10]

Komponenten

5

Versuchsvorschrift

A rapidly stirred solution of 15.5 grams (0.074 mole) of 2-bromo-4-chlorophenol, 20.0 grams (0.145 mole) of anhydrous powdered potassium carbonate, and 10 mL (0.106 mole) of dimethyl sulfate in 150 mL of acetone was heated at reflux for about 18 hours. After this time, the reaction mixture was concentrated under reduced pressure to a residue. The residue was partitioned between 100 mL each of water and methylene chloride. The organic layer was removed and washed with an aqueous solution saturated with sodium chloride. The organic layer was then dried with magnesium sulfate and filtered. The filtrate was passed through a short column of silica gel. Elution was accomplished with 500 mL of methylene chloride. The eluate was concentrated under reduced pressure, yielding 16.3 grams of 3-bromo-4-methoxychlorobenzene. The NMR spectrum was consistent with the proposed structure.

Aufarbeitung

  1. temperatureat reflux for about 18 hours
  2. concentrationAfter this time, the reaction mixture was concentrated under reduced pressure to a residue
  3. customThe residue was partitioned between 100 mL each of water and methylene chloride
  4. customThe organic layer was removed
  5. washwashed with an aqueous solution saturated with sodium chloride
  6. dry with materialThe organic layer was then dried with magnesium sulfate
  7. filtrationfiltered
  8. washElution
  9. concentrationThe eluate was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-e47ef83115aa490e84a80898ca6b9c2d
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05616718

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