Chemical Forums
Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: soliman on January 25, 2008, 03:53:07 PM
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please;
procedure for preparation of:
2,6- naphthalene dicarbonyldichloride and 2,6- dichloro carbonyl pyridine
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http://www.chemicalforums.com/index.php?topic=22234.msg85057#msg85057
http://www.chemicalforums.com/index.php?topic=22236.msg85058#msg85058
http://www.chemicalforums.com/index.php?topic=22237.msg85060#msg85060
http://www.chemicalforums.com/index.php?topic=22234.msg85064#msg85064
http://www.chemicalforums.com/index.php?topic=22241.msg85075#msg85075
Don't you think 1 post is enough?
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I can't understand , what do you want from this links
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I can't understand , what do you want from this links
Please read forum rules (http://www.chemicalforums.com/index.php?page=forumrules). Don't crosspost.
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You can synthesize pyridine-2,6-dicarbonyl dichloride with the Hantzsch pyridine synthesis.
http://en.wikipedia.org/wiki/Hantzsch_pyridine_synthesis
Hydrolysis of the ester and conversion to the acyl chloride yields your product.
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thank you for reply
but i need 2,6-dicarboxylic acid pyridine this meyhode give 3,5 dicarboxylic
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thank you for reply
but i need 2,6-dicarboxylic acid pyridine this meyhode give 3,5 dicarboxylic
no one cares
you should do your own research
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thank you for reply
but i need 2,6-dicarboxylic acid pyridine this meyhode give 3,5 dicarboxylic
oops my bad... you can oxidize 2,6-lutidine (commercially available) using potassium permanganate.
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I'm not student , but i interset in this topic
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I'm not student , but i interset in this topic
Just out of curiosity, why is this compound of such interest to you? If you are not a student, and you don't seem to someone in the professional fields related, so...
But really, what is special about this compound that you so desperately need to know?
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Thanks all for helping me and speacially thanks for Mr .macman104 for his curiosity