反应 #2460314

ord-806025c519304284a704b55dca7b89bd

反应方程式

CC(C)(C)[O-].[Na+]
sodium tert-butoxide
CCCCc1ccc(N)cc1
4-n-butyl aniline
Brc1ccc(/C=C/c2ccc(Br)cc2)cc1
trans-4,4′-dibromostilbene
CCCCc1ccc(Nc2ccc(/C=C/c3ccc(Nc4ccc(CCCC)cc4)cc3)cc2)cc1
trans-4,4′-di(p-n-butylphenyl)aminostilbene

溶剂

反应条件

温度
90°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他The solid was collected
  2. 2
    洗涤washed three times with methanol and ether
  3. 3
    其他isolated in 68.8% (1.93 g)
  4. 4
    其他yield as an NAM-pure product

实验过程

To a solution of tris(di-benzylideneacetone)dipalladium (Pd2(dba)3) (0.335 g, 0.365 mmol) and bis-(diphenylphosphino)ferrocene (DPPF) (0.294 g, 0.530 mmol) in dry toluene (20 ml) under nitrogen atmosphere was added trans-4,4′-dibromostilbene (10) (2.0 g, 5.91 mmol) at room temperature, and the resultant mixture was stirred for 10 min, sodium tert-butoxide (2.6 g) and 4-n-butyl aniline (1.77 g, 11.83 mmol) were added to this solution and stirred at 90° C. overnight. The solid was collected, washed three times with methanol and ether, and isolated in 68.8% (1.93 g) yield as an NAM-pure product. 1H NMR (CDCl3, 500 MHz) δ ppm: 7.38 (d, J=8.0 Hz, 4H), 7.10 (d, J=8.5 Hz, 4H), 7.03 (d, J=8.0 Hz, 4H), 7.0 (d, J=8.5 Hz, 4H), 6.91 (s, 2H, ═CH), 5.77 (s, 2H, NH), 2.56 (t, J=7.7 Hz, CH2, 4H), 1.59 (m, CH2, 4H), 1.37 (m, CH2, 4H), 0.94 (t, J=7.5Hz, CH3, 6H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07459106B2uspto-grants-2008_12