Eddygp
National Hazard
Posts: 858
Registered: 31-3-2012
Location: University of York, UK
Member Is Offline
Mood: Organometallic
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Interesting primary amide to nitrile conversion
These authors have shown a facile and extremely quick (1 min) conversion from nitriles to primary amides and viceversa, using ZnCl2 and
microwaves.
I'm not entirely sure what the scope of this reaction is likely to be, but I doubt there would be many side reactions for most common functional
groups (maybe apart from ester hydrolysis).
It is unlikely that something like this gets any better for a home chemist: ZnCl2, water, tetrahydrofuran and acetamide is all that is needed.
While I don't have any projects myself regarding this, I was wondering if someone has been thinking of this lately.
there may be bugs in gfind
[ˌɛdidʒiˈpiː] IPA pronunciation for my Username |
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Chemi Pharma
Hazard to Others
Posts: 349
Registered: 5-5-2016
Location: Latin America
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Mood: Quarantined
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Nowadays, different methods were discovered to dehydrate an amide to nitrile, not only ZnCl2 and aquous THF.
Here's the paper I have, attached below, that tells what everybody want to know about the recent discovered methods to do this, including what about
@Eddygp said:
Attachment: amides to nitriles - various methods.pdf (106kB)
This file has been downloaded 464 times
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zed
International Hazard
Posts: 2277
Registered: 6-9-2008
Location: Great State of Jefferson, City of Portland
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Mood: Semi-repentant Sith Lord
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Well, yes. I have been thinking about dehydration of Amides to Nitriles recently.
Were Indole-Acetonitrile easily synthesized form Indole Acetamide, interesting possibilities might emerge.
Indoles are so fussy though.
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