Hydrochloric Acid → 1-Bromo-3,5-dichloro-2-methoxybenzene

HRID 2100358Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2100358
[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Cl:9])[C:3]=1[OH:10].[C:11](=O)([O-])[O-].[K+].[K+].CI.Cl>CC(C)=O>[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Cl:9])[C:3]=1[O:10][CH3:11]

Komponenten

6

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

2-Bromo-4,6-dichlorophenol (Preparation 24, 4.6 g, 19 mmol), potassium carbonate (4.5 g, 32.3 mmol) and methyl iodide (1.8 ml, 20.5 mmol) were combined in 46 ml acetone and heated to reflux for 18 hours. The reaction was cooled to 0° C., 1N HCl (aqueous) was added to give pH 3, and the reaction was extracted into 50 ml ethyl acetate. The organic layer was washed with brine (2×20 ml), dried over sodium sulphate and concentrated in vacuo to afford the title compound as a brown solid (5.5 g).

Aufarbeitung

  1. temperatureheated
  2. temperatureto reflux for 18 hours
  3. customto give pH 3
  4. extractionthe reaction was extracted into 50 ml ethyl acetate
  5. washThe organic layer was washed with brine (2×20 ml)
  6. dry with materialdried over sodium sulphate
  7. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-e270c987cee64043a33661ecb3fdd6d6
Quelldatensatz
uspto-grants-2009_08
Patentnummer
US07572797B2

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