Diethyl Ether → 3-Fluoro-p-anisaldehyde

HRID 1955714Notes

Reaction equation

HRID 1955714 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][CH3:9].C[CH2:11][O:12]CC>C(Cl)Cl.[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:11]=[O:12]

Participants

5

Procedure

To a solution of o-fluoroanisole, 101 g (0.80 mol) in 50 ml dry methylene chloride is added dropwise over 30 minute a solution of titanium tetrachloride, 182 g (0.96 mol, 1.2 equiv.) and α,α-dichloromethylmethyl ether, 110 g (0.96 mol) 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 one hour longer, and then poured over crushed ice-water with stirring. Ether (1 l) is added, and the mixture is stirred under nitrogen until solution occurs. The organic layer is extracted with water, sodium bicarbonate solution and is dried (MgSO4). The solvent is evaporated at 30° to leave crude product as an oil. When vacuum distilled through a jacketed Vigreux column, the oil 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

  1. temperatureThe temperature is maintained at 10°-20° C. with an ice-bath
  2. additionpoured
  3. stirringwith stirring
  4. stirringthe mixture is stirred under nitrogen until solution
  5. extractionThe organic layer is extracted with water, sodium bicarbonate solution
  6. dry with materialis dried (MgSO4)
  7. customThe solvent is evaporated at 30°
  8. customto leave crude product as an oil
  9. distillationWhen vacuum distilled through a jacketed Vigreux column

Sources & evidence

ORD record
ord-96c0619b15b845b8a0ad39dd6e05d04f
Source dataset
uspto-grants-1998_07
Patent number
US05776962

Reaction notes

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