반응 #1256716

ord-f85afddd930841fabddb2b6d70317912

반응 방정식

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
수율 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
수율 95.5%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07824582B2uspto-grants-2010_11