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Topic: Schlosser Modification  (Read 3149 times)

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Offline AlphaScent

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Schlosser Modification
« on: January 03, 2014, 11:39:34 AM »
The paper I have says using phenyllithium is the base to use.  It does not explain why.  Would you guys think using n-butyllithium could be used in its place?  Phenyllithium is less basic but it is negligible in my opinion.

What are your thoughts?
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Offline discodermolide

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Re: Schlosser Modification
« Reply #1 on: January 03, 2014, 11:57:26 AM »
In the original publication Schlosser himself suggests phenyl lithium or butyllithium. So try butyllithium.
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Offline TheUnassuming

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Re: Schlosser Modification
« Reply #2 on: January 03, 2014, 12:34:59 PM »
Agreed, give it a try! 
Quick wiki check looks like E. J. Corey used n-BuLi back in the 70's for the Schlosser Modification.
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Offline discodermolide

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Re: Schlosser Modification
« Reply #3 on: January 03, 2014, 12:54:36 PM »
So it has the Corey seal of approval. It is guaranteed to work then!
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Offline AlphaScent

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Re: Schlosser Modification
« Reply #4 on: January 03, 2014, 02:01:55 PM »
Disco,

The paper does say that!! Awesome.  Wiley is being a huge pain in the butt with me being able to see the whole publication.  All I see is the procedure and he only says phenyllithium.  Thank you again for everything.

I saw the Corey work, but that is allylic alcohols.  Did not want to assume.

But hell, youre right! If Corey does it, it is gospel!

Ha, thanks guys.

I will post results later.
If you're not part of the solution, then you're part of the precipitate

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