Methane, dichloromethoxy- → 5-Chloro-2-methoxy-3-methylbenzaldehyde

HRID 1462004Notes

Reaction equation

HRID 1462004 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([O:8]C)=[C:4]([CH3:10])[CH:3]=1.[CH3:11][O:12][CH:13](Cl)Cl.C(=O)(O)[O-].[Na+]>C(Cl)Cl.[Ti](Cl)(Cl)(Cl)Cl>[Cl:1][C:2]1[CH:3]=[C:4]([CH3:10])[C:13]([O:12][CH3:11])=[C:6]([CH:7]=1)[CH:5]=[O:8]

Participants

6

Conditions

Temperature
0 °C

Procedure

Titanium tetrachloride (24.3 g, 0.128 mole) is added to a solution of 4-chloro-2-methylanisole (10 g, 0.064 mol) in methylene chloride (150 ml) at 0° C. alpha,alpha-Dichloromethyl methyl ether (8.04 g, 0.070 mol) was then added dropwise with stirring over a three minute period at 0° C. The mixture was stirred for 30 minutes at 0° C. then poured into a saturated aqueous solution of sodium bicarbonate (700 ml). The organic layer was then separated and the aqueous phase extracted with methylene chloride. The combined organic extracts were washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was chromatographed on a silica gel (300 g) column using hexane-ether (6-1) as eluent. Fractions of 15 ml each were collected. Fractions 21-50 were combined and evaporated in vacuo to a white solid (8.9 g). This solid was rechromatographed on silica gel (300 g), eluting with hexane (15 ml fractions). Fractions 174-215 were combined and evaporated in vacuo to give 2.1 g of the title product as a white solid.

Workup

  1. additionwas then added dropwise
  2. stirringThe mixture was stirred for 30 minutes at 0° C.
  3. customThe organic layer was then separated
  4. extractionthe aqueous phase extracted with methylene chloride
  5. washThe combined organic extracts were washed with brine
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo
  8. customThe residue was chromatographed on a silica gel (300 g) column
  9. customFractions of 15 ml each were collected
  10. customevaporated in vacuo to a white solid (8.9 g)
  11. customThis solid was rechromatographed on silica gel (300 g)
  12. washeluting with hexane (15 ml fractions)
  13. customevaporated in vacuo

Sources & evidence

ORD record
ord-4451c410b8c14050a7d5d49421f5de85
Source dataset
uspto-grants-1984_07
Patent number
US04457939

Reaction notes

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