no. no funcionará... "¿por qué?"
¡porque lo que es el elemento utilizado en esta reacción, es el aluminio !
el trabajo del mercurio es crear una amalgama. y de esta manera quitar la capa de "alumina (la oxidacion natural del aire sobre el aluminio")
-para otras maneras a una amina es :
*LiAlH4 (hidruro de aluminio de litio), menos tóxico, bastante inestable / difícil de encontrar.... fácil si usted es una causa profesional es uno de la reducción más fácil.
*o la pareja Zn/Ni pero he probado este método
si alguien tiene otra informacion seria bueno compartirla aqui tambien.
¡porque lo que es el elemento utilizado en esta reacción, es el aluminio !
el trabajo del mercurio es crear una amalgama. y de esta manera quitar la capa de "alumina (la oxidacion natural del aire sobre el aluminio")
-para otras maneras a una amina es :
*LiAlH4 (hidruro de aluminio de litio), menos tóxico, bastante inestable / difícil de encontrar.... fácil si usted es una causa profesional es uno de la reducción más fácil.
*o la pareja Zn/Ni pero he probado este método
si alguien tiene otra informacion seria bueno compartirla aqui tambien.
- By waltjr5858
Actually the lithium aluminum hydride is absolutely not the easiest reduction. I have hundreds of grams of that stuff and it's very easy to buy. I followed protocol exact same Reaction Time same exact amounts and the product is at best a 30% yield and it is all kinds of mixed with side products... yes it will reduce the double bond and the Nitro group but it leaves behind a ton of oxime... hydroxylamine and whatever else. I think the best reduction is the aluminum amalgam but that reaction is extremely finicky and if you can't get the amalgam perfect it won't go. Then we have the copper and borohydride which is great but I found that the laurelhydride has to be pretty damn fresh.
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- By waltjr5858
Borohydride.... I have definitely wasted hundreds of grams of p2np on all different type of reactions. Another fairly clean way which is posted on this site is using zinc but the directions as they are posted do not work and I believe the poster that put them up said he just found them on the Internet and was going to give them a try. Using tin 2 chloride well absolutely give high yields of ketoxime and absolutely no acid needs to be added just the tin and the p2np. Allow that to run for maybe an hour or so and the exothermic reaction will come back to room temperature and you can kind of use their instructions for extraction for the next step. The Next Step requires an adjustment from what they put otherwise yes the oxime will go to amine but the double bond will remain. Use zinc and glacial acetic acid but take it up to reflux for 4 hours and that will saturate the double bond. A lot of write-ups say it will tolerate the double bond but they are also only doing 5 minute reactions to reduce the oxime to Amine and leaving the double bond. Another poster on the reaction on here somewhere used glacial acetic acid and a little bit of HCL when he did it and was successful. I tried it both ways with a dash of HCL on one maybe 10 mL to the whole reaction and just with GAA. Both fully successful. But more work than the aluminum amalgam. Although that damn amalgam can be tough to get right