Diethyl Ether → 3-Fluoro-p-anisaldehyde
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][CH3:9].C(Cl)Cl.C[CH2:14][O:15]CC>[Ti](Cl)(Cl)(Cl)Cl>[F:1][C:2]1[CH:7]=[C:6]([CH:5]=[CH:4][C:3]=1[O:8][CH3:9])[CH:14]=[O:15]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of o-fluoroanisole, 101 g. (0.80 mole) in 500 ml. dry methylene chloride is added dropwise over 30 minutes a solution of titanium tetrachloride, 182 g. (0.96 mole, 1.2 equiv.) and α,α-dichloromethylmethyl ether, 110 g. (0.96 mole) in an equal volume of methylene chloride. The temperature is maintained at 10°-20° C. with an ice-bath. The mixture is stirred at room temperature for 1 hour longer and then poured over crushed ice-water with stirring. Ether (1 l.) is added, and the mixture stirred under nitrogen until solution occurs. The organic layer is extracted with water (3×), sodium bicarbonate solution (3×) and dried (MgSO4). The solvent is evaporated off at 30° to give crude product as an oil. The oil is vacuum distilled through a jacketed Vigreux column when it gives 3-fluoro-4-methoxybenzaldehyde, B.P. 120°-121° C., at 10 mm. Hg; Rf 0.6 on a silica-gel G plate with methylene chloride.
Workup
- temperatureThe temperature is maintained at 10°-20° C. with an ice-bath
- additionpoured
- stirringwith stirring
- stirringthe mixture stirred under nitrogen until solution
- extractionThe organic layer is extracted with water (3×), sodium bicarbonate solution (3×)
- dry with materialdried (MgSO4)
- customThe solvent is evaporated off at 30°
- customto give crude product as an oil
- distillationdistilled through a jacketed Vigreux column when it
Sources & evidence
- ORD record
- ord-be6524fd1c0044f296996824ff7dc163
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05643959
Reaction notes
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