April 24, 2024, 08:09:33 PM
Forum Rules: Read This Before Posting


Topic: N-Arylation of Theophylline  (Read 1536 times)

0 Members and 1 Guest are viewing this topic.

Offline lfga94

  • Very New Member
  • *
  • Posts: 1
  • Mole Snacks: +0/-0
N-Arylation of Theophylline
« on: October 10, 2017, 07:16:46 PM »
Hello everybody!

I'm working on the N-arylation of theophylline, a methylxanthine. I'm using theophylline and 2-chloropyridine as substrate, K3PO4 as the base, CuI as catalyst and TMEDA as the co-ligand (to stabilize the copper). The solvent is DMF and I'm working with inert atmosphere. After the reaction, a solid remains in the bottom; it seems orange but when I filter and wash it, it turns gray. I was wondering if anybody have an idea of what it could be. It isn't the product of interest, I obtain it from the extraction of the solution.

Offline pgk

  • Chemist
  • Full Member
  • *
  • Posts: 892
  • Mole Snacks: +97/-24
Re: N-Arylation of Theophylline
« Reply #1 on: October 11, 2017, 09:27:32 AM »
Either you have formed an insoluble copper(I)-theophylline complex that changes color after washing, by clustering molecules of the washing solvent (water?); or you have formed an Ullmann dimerization product (CuI/TMEDA in hot DMF) that changes color, under neutral conditions. But you can verify it by taking a 1H-NMR spectrum.
« Last Edit: October 11, 2017, 12:45:30 PM by pgk »

Sponsored Links