cactusmae
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selective reduce nitroaromatics
I finially figured out the problem with my reduction with nitroaromatics with Iron and HCl. The problem is that I have a substitute with dihylogenated
double bond CFBr-CF2Br. When I tried to reduce nitro group into amine with Iron, it is also dehylogenated CFBr-CF2Br and finally give a mixture. Any
suggestion of reduce agent, which won't dehylogenated the compound?
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Dr.Bob
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Sodium dithionate might work. That is an interesting compound you've got.
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UnintentionalChaos
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That perhalogenated alkyl chain is going to be mighty reactive...when and if you can reduce the nitro group to an amine, I'd expect it to react
immediately with the bromines on the sidechain. You could probably get away with reducing the nitro group on a nitrophenyltrifluoroethylene, but you
wouldn't be able to brominate the product without serious issues.
Department of Redundancy Department - Now with paperwork!
'In organic synthesis, we call decomposition products "crap", however this is not a IUPAC approved nomenclature.' -Nicodem
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cactusmae
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I tried sodium polysulfide once. It is not working. I am not sure why. Because without the CFBrCF2Br, it works fine with just perfluoroalkyl chain.
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smuv
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I recommend.hydrogenation w. adams catalyst in thf.
"Titanium tetrachloride…You sly temptress." --Walter Bishop
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Organikum
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You will have to find out the conditions under which reduction still takes place but your functional group stays unharmed.
There are several articles where the authors claim very selective reductions, which will do it for you only experiment can schow.
Attached are references for iron and tin and on the Zinin reaction with sulfides. There was another one with iron and CaCl2 which cannot find now, it
was simply like it says and no HCl. Iron must be properly activated I suppose or not much will happen.
My personal bet would be on the SnCl2.
[Edited on 17-2-2012 by Organikum]
Attachment: Sulfide.zip (1.1MB)
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