Phosphorus oxychloride → 3-Methyl-5-phenyl-2,4-pentadienoic acid

HRID 1176100

Reaktionsgleichung

Reaktionsgleichung von HRID 1176100
P(Cl)(Cl)(Cl)=O.[C:6]1([CH:12]=[CH:13][C:14]([CH3:17])(O)[CH3:15])[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[C:18]([O-:21])(=[O:20])C.[Na+]>CN(C)C=O.O>[CH3:15][C:14]([CH:13]=[CH:12][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[CH:17][C:18]([OH:21])=[O:20]

Komponenten

6

Versuchsvorschrift

Dimethylformamide (DMF, anhydrous, 25 mL) was cooled to 0-5° C. and phosphorus oxychloride (16.4 mL) was added dropwise over a period of an hour. The resulting solution was added dropwise to a cooled (0-5° C.) solution of 4-phenyl-2-methyl-3-buten-2-ol (0.14 mol) in 60 mL of anhydrous DMF over a period of an hour. The reaction mixture was then warmed to room temperature, gradually heated up to 80° C., stirred at 80° C. for three hours and cooled to 0-5° C. To the cooled reaction solution was added dropwise a solution of sodium acetate (80 g) in deionized water (190 mL) over a period of two hours. The mixture was then reheated to 80° C., stirred at 80° C. for an additional 10 minutes, cooled down to room temperature and extracted with ether (300 mL) twice. The combined extract was washed with water (200 mL), dried over anhydrous sodium sulfate, filtered and concentrated in vacuum to yield 16.7 g of the desired 3-methyl-5-phenyl-2,4-pentadienal as a liquid which was used in the next step without further purification.

Aufarbeitung

  1. additionThe resulting solution was added dropwise to
  2. temperaturegradually heated up to 80° C.
  3. temperaturecooled to 0-5° C
  4. customTo the cooled reaction solution
  5. customwas then reheated to 80° C.
  6. stirringstirred at 80° C. for an additional 10 minutes
  7. temperaturecooled down to room temperature
  8. extractionextracted with ether (300 mL) twice
  9. extractionThe combined extract
  10. washwas washed with water (200 mL)
  11. dry with materialdried over anhydrous sodium sulfate
  12. filtrationfiltered
  13. concentrationconcentrated in vacuum

Quellen und Nachweise

ORD-Eintrag
ord-910c52e50f3544bb99532884d2a6fe7e
Quelldatensatz
uspto-grants-2010_11
Patentnummer
US07842727B2

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