Rich_Insane
Hazard to Others
Posts: 371
Registered: 24-4-2009
Location: Portland, Oregon
Member Is Offline
Mood: alive
|
|
Protonation of oximes
Hey everyone. I have no formal organic chemistry education, so forgive me if this a very basic question.
Let's say I have an aldoxime that is heated beyond its melting point and is in solution. What I was wondering is whether it is possible to protonate
the oxygen on the aldoxime and then have the unstable (-OH2+) and the extra hydrogen come off as H3O+, thus regenerating the acid. The result is a
nitrile.
In this case, I was thinking of using p-TsOH, as it is a very strong organic acid.
Is this mechanism feasible, or will the initial protonation of the nitrogen screw up the entire process?
My reasoning behind this is that a common method of forming nitriles from oximes is heating the oxime with acetic anhydride. I am not sure if the
process occurs by anhydride's dehydration of the oxime or if the oxime oxygen is acetylated and then leaves as acetic acid... If this idea of
protonating the oxime oxygen is absolutely ridiculous, would it be possible to substitute acetic anhydride with a less risky acid anhydride such as
phthalic anhydride?
I should also note that I plan to carry out this process in DCM or a very volatile solvent. After the reaction completes, I want to boil away the
solvent and wash with water to remove phthalic acid and then use a method of oxidative hydration to form the amide.
|
|
Rich_Insane
Hazard to Others
Posts: 371
Registered: 24-4-2009
Location: Portland, Oregon
Member Is Offline
Mood: alive
|
|
I'm guessing that this is a really stupid question.
|
|
eidolonicaurum
Hazard to Self
Posts: 71
Registered: 2-1-2014
Location: Area 51
Member Is Offline
Mood: Hydric
|
|
I would answer the question myself, but I do not know the answer. Almost all questions, no matter how stupid, are answered.
|
|
Metacelsus
International Hazard
Posts: 2539
Registered: 26-12-2012
Location: Boston, MA
Member Is Offline
Mood: Double, double, toil and trouble
|
|
https://en.wikipedia.org/wiki/Nitrile#Dehydration_of_amides_...
Many, many reagents can do this, and new ones are constantly being developed:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2935138/
Phthalic anhydride and acetic anhydride are very different beasts. I am not sure your scheme would work.
Edit: This should probably be merged with Rich_Insane's previous thread on this subject:
http://www.sciencemadness.org/talk/viewthread.php?tid=26038
[Edited on 10-1-2014 by Cheddite Cheese]
|
|