January 11, 2025, 06:52:16 PM
Forum Rules: Read This Before Posting


Topic: aromatic Nucleophillic substitution  (Read 5919 times)

0 Members and 1 Guest are viewing this topic.

Offline ANDLOS

  • Regular Member
  • ***
  • Posts: 17
  • Mole Snacks: +0/-2
aromatic Nucleophillic substitution
« on: August 24, 2009, 12:00:51 PM »
i want to know best condition for aromatic Nucleophillic substitution  of chloro with secondary cyclic amine in
4-chloro-3-nitrobenzoate ester

Offline Borek

  • Mr. pH
  • Administrator
  • Deity Member
  • *
  • Posts: 27895
  • Mole Snacks: +1816/-412
  • Gender: Male
  • I am known to be occasionally wrong.
    • Chembuddy
Re: aromatic Nucleophillic substitution
« Reply #1 on: August 24, 2009, 12:09:12 PM »
ChemBuddy chemical calculators - stoichiometry, pH, concentration, buffer preparation, titrations.info

Offline ANDLOS

  • Regular Member
  • ***
  • Posts: 17
  • Mole Snacks: +0/-2
Re: aromatic Nucleophillic substitution
« Reply #2 on: August 24, 2009, 03:47:26 PM »
do i make any mistake please explain to me i read rules and i do not find any thing wrong i do

Offline Arctic-Nation

  • Chemist
  • Full Member
  • *
  • Posts: 265
  • Mole Snacks: +33/-9
Re: aromatic Nucleophillic substitution
« Reply #3 on: August 24, 2009, 05:24:24 PM »
Forum rules state that you should have made an effort in solving the problem yourself before asking for help. In your case, you should have tried the reaction and/or searched for some relevant procedures.

That aside, how about K2CO3 in DMF?

Offline kiwi

  • Chemist
  • Full Member
  • *
  • Posts: 229
  • Mole Snacks: +20/-0
  • Gender: Male
Re: aromatic Nucleophillic substitution
« Reply #4 on: August 25, 2009, 06:11:10 AM »
why don't you do a Buchwald-Hartwig coupling instead?

http://www.organic-chemistry.org/namedreactions/buchwald-hartwig-reaction.shtm

Offline ANDLOS

  • Regular Member
  • ***
  • Posts: 17
  • Mole Snacks: +0/-2
Re: aromatic Nucleophillic substitution
« Reply #5 on: August 28, 2009, 11:38:20 AM »
I try reaction dmso in k2co3
but there is a strong froth after 24 hr stirring at 70 is this reaction condition optimum??

Offline ANDLOS

  • Regular Member
  • ***
  • Posts: 17
  • Mole Snacks: +0/-2
Re: aromatic Nucleophillic substitution
« Reply #6 on: August 28, 2009, 11:40:59 AM »
why don't you do a Buchwald-Hartwig coupling instead?

http://www.organic-chemistry.org/namedreactions/buchwald-hartwig-reaction.shtm

the reagent of this reaction not available at my college and very expensive

Offline Arctic-Nation

  • Chemist
  • Full Member
  • *
  • Posts: 265
  • Mole Snacks: +33/-9
Re: aromatic Nucleophillic substitution
« Reply #7 on: August 28, 2009, 03:30:40 PM »
Do you have any analytical equipment you can use to check the progress of your reaction?

And the basic Pd compounds aren't that expensive. You only need a few milligrams, and if properly stored most of them last for at least a year.

Offline ANDLOS

  • Regular Member
  • ***
  • Posts: 17
  • Mole Snacks: +0/-2
Re: aromatic Nucleophillic substitution
« Reply #8 on: August 29, 2009, 12:28:13 PM »
Do you have any analytical equipment you can use to check the progress of your reaction?

And the basic Pd compounds aren't that expensive. You only need a few milligrams, and if properly stored most of them last for at least a year.
i check progress of reaction by tlc, mp

Sponsored Links