反应 #1256716

ord-f85afddd930841fabddb2b6d70317912

反应方程式

Cl
HCl
[H-].[Na+]
NaH
N#CCC#N
malononitrile
Cc1cncc(C)c1-c1c(C)cc(I)cc1C
11
Cc1cncc(C)c1-c1c(C)cc(I)cc1C
4-(4-iodo-2,6-dimethyl-phenyl)-3,5-dimethyl-pyridine
Cc1cncc(C)c1-c1c(C)cc(C(C#N)C#N)cc1C
title compound
收率 95.5%
Cc1cncc(C)c1-c1c(C)cc(C(C#N)C#N)cc1C
2-[4-(3,5-dimethyl-pyridin-4-yl)-3,5-dimethyl-phenyl]-malononitrile
收率 95.5%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGThe reaction mixture was next stirred at 85° C. under N2 for 5 h
  2. 2
    其他The solvent was then removed under reduced pressure
  3. 3
    洗涤The resulting solid was washed with benzene (20 mL)
  4. 4
    workup.DISSOLUTIONdissolved in water
  5. 5
    过滤filtered
  6. 6
    其他to give a dark-yellow aqueous solution
  7. 7
    过滤the resulting yellow precipitate was collected by filtration
  8. 8
    其他to give an orange solid
  9. 9
    其他The crude product was purified by flash chromatography on silica gel eluting with 1:1 hexane

实验过程

To an ice-cooled suspension of NaH (0.12 g, 5.0 mmol) in anhydrous 1,2-dimethoxyethane (8 mL) was added dropwise via syringe a solution of malononitrile (0.165 g, 2.50 mmol) in anhydrous 1,2-dimethoxyethane (2 mL) under N2. The mixture was stirred for 1 h at room temperature under N2. Next, 11 (0.674 g, 2.00 mmol) and tetrakis(triphenyphophine)palladium(0) (0.232 g, 0.200 mmol) were added to the resulting pink suspension under an N2 flow. The reaction mixture was next stirred at 85° C. under N2 for 5 h. The solvent was then removed under reduced pressure. The resulting solid was washed with benzene (20 mL), dissolved in water, and filtered to give a dark-yellow aqueous solution. This solution was neutralized with 5% HCl to pH=7, and the resulting yellow precipitate was collected by filtration to give an orange solid. The crude product was purified by flash chromatography on silica gel eluting with 1:1 hexane: ethyl acetate, to give 0.525 g (95.5%) of the title compound as red solid: mp 58-60° C.; 1H NMR (400 MHz, CDCl3): δ 8.412 (s, 2H), 7.286 (s, 2H), 5.100 (s, 1H), 1.946 (s, 6H), 1.895 (s, 6H); 13C NMR (100 MHz, CDCl3): δ 149.066, 146.564, 139.513, 137.283, 130.441, 126.692, 125.518, 112.024,28.059, 19.988, 16.704; Anal. Calcd. for C18H17N3·H2O: C, 73.69; H, 6.53; N, 14.32. Found; C, 73.36; H, 6.35; N, 14.07.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07824582B2uspto-grants-2010_11