2-Bromo-1,1-dimethoxyethane → HCID 67157111, compound
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]=1Participants
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
- temperatureunder cooling with ice
- temperatureheated
- temperatureto reflux for five hours
- concentrationThe reaction mixture was concentrated under reduced pressure, and cold water
- additionwas added
- extractionThe resulting mixture was extracted with ether
- washthe organic layer was washed with a saturated sodium chloride aqueous solution
- dry with materialdried with sodium sulfate
- filtrationAfter filtration
- distillationthe solvent was distilled under reduced pressure
- 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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