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Topic: reduction of ketones to alkanes  (Read 6226 times)

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Offline lithiumuranium

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reduction of ketones to alkanes
« on: May 24, 2012, 09:37:16 AM »
Can H2, Pd (high pressure) be used to reduce a non-aryl ketone to an alkane, when other groups are too sensitive to use clemmensen or wolff-kishner reduction?

Offline discodermolide

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Re: reduction of ketones to alkanes
« Reply #1 on: May 24, 2012, 09:52:11 AM »
Can H2, Pd (high pressure) be used to reduce a non-aryl ketone to an alkane, when other groups are too sensitive to use clemmensen or wolff-kishner reduction?


I found this reference:
Poly(ethylene glycol) (PEG) (400) has been found to be a superior solvent over ionic liquids by severalfold in promoting the hydrogenation of various functional groups using Adams' catalyst. Both the catalyst and PEG were recycled efficiently over 10 runs without loss of activity, and without substrate cross contamination.
S. Chandrasekhar, S. Y. Prakash, C. L. Rao, J. Org. Chem., 2006, 71, 2196-2199.

on this page: http://www.organic-chemistry.org/synthesis/C1H/reductionsalkenes.shtm
the 10th reference down the page.
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Offline Dan

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Re: reduction of ketones to alkanes
« Reply #2 on: May 24, 2012, 03:54:54 PM »
What about Mozingo reduction?
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Offline orgopete

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Re: reduction of ketones to alkanes
« Reply #3 on: May 24, 2012, 04:24:14 PM »
What about Mozingo reduction?

I agree.
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Offline lithiumuranium

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Re: reduction of ketones to alkanes
« Reply #4 on: May 24, 2012, 09:50:09 PM »
This is where I got the question from http://www.icho2012.org/44th_International_Chemistry_Olympiad_Preparatory_Problems.pdf (page 45).

In the reaction from [F] to [G], it is apparent that the ketone gets reduced to a methylene group if you look at the product that comes after . However, I thought that H2, Pd reduced ketones to alcohols only. So I didn't understand why they used catalytic hydrogenation (does it also work in this case?) when this is a clemmensen reduction.

this is my solution: http://postimage.org/image/d112bxme9/168e3932/

Offline Dan

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Re: reduction of ketones to alkanes
« Reply #5 on: May 25, 2012, 03:33:45 AM »
This is where I got the question from http://www.icho2012.org/44th_International_Chemistry_Olympiad_Preparatory_Problems.pdf (page 45).

Haha, there's ~4 months of my PhD on p46/47!

Back to topic: I think what we are seeing here is reduction of the ketone to an benzylic alcohol. Generally the RCH2-OH is not cleaved by H2, Pd - but if R is an aromatic group then it is cleaved (hydrogenolysis). Benzyl (CH2Ph) ethers are commonly used as alcohol protecting groups because they are easily cleaved this way.

Protecting group cheimistry:

PhCH2-OR + H2 (Pd cat.) :rarrow: PhCH3 + HOR

This example:

ArC=O(R) + H2 (Pd cat.) :rarrow: ArC-OH(H)(R)
ArC-OH(H)(R) + H2 (Pd cat.) :rarrow: ArCH2R + H2O
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