Water → 4-(2-Bromoethyl)benzaldehyde
Reaction equation
C[O:2][CH:3](Cl)Cl.[CH2:6]([Br:14])[CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.O>C(Cl)Cl.[Ti](Cl)(Cl)(Cl)Cl>[Br:14][CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][C:11]([CH:3]=[O:2])=[CH:10][CH:9]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of dichloromethyl methyl ether (62 ml) in methylene chloride (40 ml) was added titanium tetrachloride (75 ml) over 10 minutes under a nitrogen atmosphere at 4-5° C. Then, a solution of phenethyl bromide (85 ml) in methylene chloride (50 ml) was added thereto over 50 minutes at 5-7° C. and the mixture was stirred for 5 hours while gradually raising the temperature of the mixture to room temperature. Water (200 ml) was added to the reaction mixture over 1 hour and the mixture was extracted with chloroform (200 ml). The chloroform layer was washed with water, a saturated aqueous sodium bicarbonate solution and saturated brine, dried over anhydrous sodium sulfate and the solvent was distilled away under reduced pressure to give a brown oily substance (167 g). The obtained brown oily substance was purified by silica gel column chromatography (eluent; hexane:ethyl acetate=20:1) to give 4-(2-bromoethyl)benzaldehyde (32.3 g) as a yellow solid, melting point 50-52° C.
Workup
- extractionthe mixture was extracted with chloroform (200 ml)
- washThe chloroform layer was washed with water
- dry with materiala saturated aqueous sodium bicarbonate solution and saturated brine, dried over anhydrous sodium sulfate
- distillationthe solvent was distilled away under reduced pressure
- customto give a brown oily substance (167 g)
- customThe obtained brown oily substance was purified by silica gel column chromatography (eluent; hexane:ethyl acetate=20:1)
Sources & evidence
- ORD record
- ord-3d9b3b405e654d558bf2048726fc352f
- Source dataset
- uspto-grants-2006_04
- Patent number
- USRE039072E1
Reaction notes
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