Methanol → 2-(2,5-dimethylphenoxymethyl)phenyl oxazol-5-yl ketone O-methyloxime

HRID 279460Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 279460
C1(C)C=CC(S([CH2:10][N+:11]#[C-:12])(=O)=O)=CC=1.[C:14](=[O:17])([O-])[O-].[K+].[K+].[CH3:20][OH:21].[CH3:22][C:23]1[CH:42]=[CH:41][C:40]([CH3:43])=[CH:39][C:24]=1[O:25][CH2:26][C:27]([CH:32]1[CH:37]=[CH:36][CH:35]=[CH:34][C:33]1=[NH:38])(OC)C=O>CCOCC>[CH3:20][O:21][N:38]=[C:33]([C:14]1[O:17][CH:12]=[N:11][CH:10]=1)[C:34]1[CH:35]=[CH:36][CH:37]=[CH:32][C:27]=1[CH2:26][O:25][C:24]1[CH:39]=[C:40]([CH3:43])[CH:41]=[CH:42][C:23]=1[CH3:22]

Komponenten

6

Versuchsvorschrift

p-Toluenesulfonylmethylisocyanide (0.23 g, 1.2 mmol), potassium carbonate (0.18 g, 1.3 mmol) and methanol (2 ml) were added to 2-(2,5-dimethylphenoxymethyl)-α-methoxy-iminophenylacetaldehyde (0.30 g, 1 mmol), and the mixture stirred under reflux for 2 hours. After completion of the reaction, ether (100 ml) was added, and the mixture was washed with brine (80 ml) twice. The ether layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate/n-hexane) and recrystallized from ethyl acetate/n-hexane to give 2-(2,5-dimethylphenoxy-methyl)phenyl oxazol-5-yl ketone O-methyloxime (0.15 g, 44.6%) as colorless crystals.

Aufarbeitung

  1. temperatureunder reflux for 2 hours
  2. additionwas added
  3. washthe mixture was washed with brine (80 ml) twice
  4. dry with materialThe ether layer was dried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by silica gel chromatography (ethyl acetate/n-hexane)
  7. customrecrystallized from ethyl acetate/n-hexane

Quellen und Nachweise

ORD-Eintrag
ord-e9c62baa3625482da461529cac07e57b
Quelldatensatz
uspto-grants-2002_03
Patentnummer
US06362212B1

Notizen zur Reaktion

Wird geladen…