تفاعل #465944

ord-84aad4bf4c1a4f86893309f2ba48179e

معادلة التفاعل

Cc1ccc(N(c2ccc(C=O)cc2)c2ccc(C)c(C)c2)cc1C
4-[N,N-bis(3,4-dimethylphenyl)amino]benzaldehyde
C[PH+](C)C.[Br-]
trimethylphosphonium bromide
[H-].[Na+]
sodium hydride
C=Cc1ccc(N(c2ccc(C)c(C)c2)c2ccc(C)c(C)c2)cc1
4-[N,N-bis(3,4-dimethylphenyl)amino]styrene
المردود 85.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىreaction at 700° C. for 5 hours
  2. 2
    ترشيحfollowed by filtration
  3. 3
    أخرىto collect a cake
  4. 4
    استخلاصThe cake was extracted with ether
  5. 5
    غسيلwashed with water
  6. 6
    أخرىthe ether was removed
  7. 7
    أخرىto obtain a crude product
  8. 8
    أخرىAfter twice recrystallized from ethanol

الإجراء التجريبي

Into a three-necked flask, 12.1 g of sodium hydride and 580 ml of 1,2-dimethoxyethane were placed, and 108.5 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, 100.0 g of 4-[N,N-bis(3,4-dimethylphenyl)amino]benzaldehyde was added to the reaction mixture, to carry out reaction at 700° C. for 5 hours, followed by filtration to collect a cake. The cake was extracted with ether and the extract was put together with the filtrate and washed with water. Then, the ether solution was dehydrated with calcium chloride, and thereafter the ether was removed to obtain a crude product. After twice recrystallized from ethanol, acicular 4-[N,N-bis(3,4-dimethylphenyl)amino]styrene was obtained in an amount of 84.5 g (yield: 85.0%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06296978B1uspto-grants-2001_10