2-Bromo-1,1-dimethoxyethane → HCID 67157111, compound

HRID 550247Notes

Reaction equation

HRID 550247 reaction equation
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([SH:9])=[CH:5][CH:4]=1)[CH3:2].Br[CH2:11][CH:12]([O:15][CH3:16])[O:13][CH3:14].CO.C[O-].[Na+]>>[CH3:14][O:13][CH:12]([O:15][CH3:16])[CH2:11][S:9][C:6]1[CH:7]=[CH:8][C:3]([CH2:1][CH3:2])=[CH:4][CH:5]=1

Participants

4

Procedure

Under a nitrogen atmosphere, 4-ethylbenzenethiol (3.50 ml, 25.4 mmol) and 2-bromo-1,1-dimethoxyethane (3.3 ml, 27.9 mmol) were added to a sodium methoxide methanol solution (0.5 M, 81.4 ml, 40.7 mmol) under cooling with ice. The reaction mixture was stirred at the same temperature for 10 minutes, and then heated to reflux for five hours. The reaction mixture was concentrated under reduced pressure, and cold water was added. The resulting mixture was extracted with ether and the organic layer was washed with a saturated sodium chloride aqueous solution and dried with sodium sulfate. After filtration, the solvent was distilled under reduced pressure and the obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:20)] to obtain the title compound (5.31 g, 93%).

Workup

  1. temperatureunder cooling with ice
  2. temperatureheated
  3. temperatureto reflux for five hours
  4. concentrationThe reaction mixture was concentrated under reduced pressure, and cold water
  5. additionwas added
  6. extractionThe resulting mixture was extracted with ether
  7. washthe organic layer was washed with a saturated sodium chloride aqueous solution
  8. dry with materialdried with sodium sulfate
  9. filtrationAfter filtration
  10. distillationthe solvent was distilled under reduced pressure
  11. customthe obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:20)]

Sources & evidence

ORD record
ord-c036b0d25d564c6ab959d5129b44405f
Source dataset
uspto-grants-2011_05
Patent number
US07943748B2

Reaction notes

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