Dimethyl Sulfate → 5-Bromo-1,2,3-trimethoxybenzene

HRID 23862

Reaktionsgleichung

Reaktionsgleichung von HRID 23862
[Br:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[C:5]([OH:10])=[C:4]([O:11][CH3:12])[CH:3]=1.[OH-].[Na+].S(OC)(O[CH3:19])(=O)=O>O.S(OC)(OC)(=O)=O>[CH3:9][O:8][C:6]1[CH:7]=[C:2]([Br:1])[CH:3]=[C:4]([O:11][CH3:12])[C:5]=1[O:10][CH3:19]

Komponenten

6

Reaktionsbedingungen

Temperatur
10 °C

Versuchsvorschrift

A mixture of 74 g (0.32 mol) of 4-bromo-2,6-dimethoxy-phenol 17 and 32 g (0.8 mol) of NaOH in 850 ml of H2O was cooled to 10° C. and 45 ml (0.48 mmol) of dimethyl sulfate was added. The mixture was refluxed for 3 h and an equal amount of dimethyl sulfate (total 0.96 mol) was then added. The mixture was refluxed for another 3 h. Upon cooling overnight, the gray product solidified and was filtered off and dissolved in 1.2 l of ether. The ether solution was filtered to remove insoluble impurity and washed sequentially with 5% NaOH solution (200 ml), water (2×200 mL), and brine (200 mL). The ether phase was dried over Na2SO4 to give a off-white solid, which was recrystallized in hexane (300 ml) to give 62.3 g (79%) of 18.

Aufarbeitung

  1. temperatureThe mixture was refluxed for 3 h
  2. temperatureThe mixture was refluxed for another 3 h
  3. temperatureUpon cooling overnight
  4. filtrationwas filtered off
  5. dissolutiondissolved in 1.2 l of ether
  6. filtrationThe ether solution was filtered
  7. customto remove insoluble impurity
  8. washwashed sequentially with 5% NaOH solution (200 ml), water (2×200 mL), and brine (200 mL)
  9. dry with materialThe ether phase was dried over Na2SO4
  10. customto give a off-white solid, which
  11. customwas recrystallized in hexane (300 ml)

Quellen und Nachweise

ORD-Eintrag
ord-8728cdf0d1c144e686d2423cb056c603
Quelldatensatz
uspto-grants-2005_02
Patentnummer
US06855657B2

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