Claisen reaction

Started by dsony2284
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dsony2284

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I have no idea about these reactions, everytime i look at them i get confused and forget. Can anyone explain the basic way to do a claisen reaction and what it incorporates. I know im asking a lot since this is online.

Thanks.
 
I have no idea about these reactions, everytime i look at them i get confused and forget. Can anyone explain the basic way to do a claisen reaction and what it incorporates. I know im asking a lot since this is online.

Thanks.

acetoacetic ester condensation is basically two mols of of esters with alpha-H's with a base that gives you beta-keto esters. since this is online and i cant draw it out, heres a picture.


claise16.gif


claise17.gif
 
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Okay just looked it up...

It requires a strong alkoxide base (strong base would result in nucleophilic addition or substitution; alkaline prevents this) and a hydronium ion (which I imagine is used to protonate the leaving alkoxy group)

Hope that's right.