반응 #465944

ord-84aad4bf4c1a4f86893309f2ba48179e

반응 방정식

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
수율 85.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타reaction at 700° C. for 5 hours
  2. 2
    여과followed by filtration
  3. 3
    기타to collect a cake
  4. 4
    추출The cake was extracted with ether
  5. 5
    세척washed with water
  6. 6
    기타the ether was removed
  7. 7
    기타to obtain a crude product
  8. 8
    기타After twice recrystallized from ethanol

실험 절차

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%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06296978B1uspto-grants-2001_10