Anisole → 2-hydroxy-alpha-(1-imidazolyl)benzaldehyde O-methyloxime

HRID 128906Notes

Reaction equation

HRID 128906 reaction equation
C1(OC)C=CC=CC=1.[Cl-].[Al+3].[Cl-].[Cl-].[CH3:13][O:14][N:15]=[C:16]([N:33]1[CH:37]=[CH:36][N:35]=[CH:34]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[O:23]CC1C=CC(Cl)=CC=1Cl>C(=O)(O)[O-].[Na+]>[CH3:13][O:14][N:15]=[C:16]([N:33]1[CH:37]=[CH:36][N:35]=[CH:34]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[OH:23]

Participants

5

Procedure

Dry anisole (6 ml) and aluminium chloride (0.59 g) were added to 2-(2,4-dichlorobenzyloxy)-α-(1-imidazolyl)benzaldehyde O-methyloxime (0.75 g), and the mixture was stirred under ice-cooling for 2 hours. After completion of the reaction, a half-saturated aqueous solution of sodium bicarbonate (100 ml) was added slowly, and the mixture was extracted with ether (50 ml) and ethyl acetate (50 ml), dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting crude product was purified by silica gel chromatography and recrystallized from ethyl acetate/n-hexane to give 2-hydroxy-α-(1-imidazolyl)benzaldehyde O-methyloxime (0.34 g) as colorless crystals. mp. 103.5°-104.5° C.

Workup

  1. temperaturecooling for 2 hours
  2. customAfter completion of the reaction
  3. extractionthe mixture was extracted with ether (50 ml) and ethyl acetate (50 ml)
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe resulting crude product was purified by silica gel chromatography
  7. customrecrystallized from ethyl acetate/n-hexane

Sources & evidence

ORD record
ord-fff4608bab8e48bda897c2cbb38ab6d5
Source dataset
uspto-grants-1995_11
Patent number
US05466661

Reaction notes

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