Réaction #465942

ord-23407fedf46f4c59937f6c2c69f9ded1

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurethe temperature was raised to 70° C.
  2. 2
    Autrereaction for 5 hours
  3. 3
    AutreThe resulting reaction solution
  4. 4
    Filtrationwas filtered
  5. 5
    Extractionthe filtrate and an ether-extract of the precipitate
  6. 6
    Lavagewashed with water
  7. 7
    Autrewas removed
  8. 8
    Autreto obtain a crude
  9. 9
    Autrereaction product
  10. 10
    AutreAfter recrystallized from ethanol

Mode opératoire

Into a three-necked flask, 14.6 g of sodium hydride and 700 ml of 1,2-dimethoxyethane were placed, and 130.8 g of trimethylphosphonium bromide was added thereto with stirring at room temperature. Next, after a drop of absolute alcohol was added, the reaction was allowed to proceed at 70° C. for 4 hours. Then, 100 g of 4-(N,N-diphenylamino)benzaldehyde was added thereto, and the temperature was raised to 70° C. to carry out reaction for 5 hours. The resulting reaction solution was filtered, and the filtrate and an ether-extract of the precipitate were put together and washed with water. Then, the ether solution was dehydrated with calcium chloride, and ether was removed to obtain a crude reaction product. After recrystallized from ethanol, acicular pale yellow vinyltriphenylamine was obtained in an amount of 83.4 g (yield: 84.0%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06296978B1uspto-grants-2001_10