Synteza metamfetaminy z P2P za pomocą Al/Hg

[Venus9987]

Witam, czy mogę użyć proszku aluminiowego 1000 zamiast folii aluminiowej?
I czy eter można zastąpić eterem naftowym?

 

[Throw-off]

Nigdy nie odniosłem sukcesu z proszkiem aluminiowym.

 

[Chemist Jun]

Proszek nie jest dobry i nie tworzy amalgamatu, ponieważ generuje wodór z dużą prędkością
Folia aluminiowa jest skuteczna, ponieważ pomaga również w przenoszeniu elektronów.

 

[Manisj@1290]

Czy mogę zastąpić etanol metanolem, aby wyprodukować metę tą metodą, ponieważ nie mam etanolu?

 

[Pinkbay]

if i cant buy diethyl ether and petroleum ether , what can i use to replace?

 

[should]

Hello sir, can we also use mercuric sulfate or mercuric iodide?

 

[William D.]

I think I used Hg iodide. But I didn't use sulfate. So one thing definitely works.

 

[should]

sir,can mercuric iodide replace mercuric chloride？ Is the dosage the same?

 

[Dephoj]

Hello,its possible to use sodium nitrate instead of sodium chloride , much thanks

 

[lalalander]

Sodium chloride is literally table salt.

 

[GhostChemist]

No
But you can try without using sodium chloride

 

[jacksprat]

Please shoot me down in flames if (good chance) I am wrong.

Has anybody attempted a one pot reduction from Pn2P via al/hg using nitromethane as methylamine source , straight to free base .

A chemical engineer out there must be able to tell me why this cannot be/ has not been done.



Thanking you in advance

 

[GhostChemist]

There were messages about this method in the discussions on the forum
But this method is dangerous

 

[Arakava]

The aqueous 39% methylamine we use in this reaction is make by this method or we can just dissolve methylamine hcl in water and add it to the mixture?

 

[HIGGS BOSSON]

You need to use aqueous methylamine freebase, which you can buy or prepare from HCL form by this method

 

[Usernator]

Hi, I need help with workup, please. I’m using steam distilled P2P made from P2NP using Fe/HCl, 40% Methylamine aq., Al pellets made from thick wire+HgCl2 and IPA as solvent. After rxn and filtering IPA, I vacuum distilled ipa from freebase, then dissolve again in ipa and bubble HCl gas thru.. pH measured and ~4-5… pour into baker, heated, but then, after almost all solvent is evaporated, mixture become dark pink/purple color and some dark purple “oil” droplets appear, also yield was only about 15%.. can sb tell me what it is or what probably I’m doing wrong? Thanks

 

[GhostChemist]

this is normal process, associated with the impure P2P
recrystallize your product

 

[Rabidreject]

Hey if I have methylamine HCl, is the only way to utilise it by freebasing and bubbling it through water to get the 39% aqueous methylamine?
Is there anyway to include it as the HCl salt and then use a weak base or something during the reduction?

 

[GhostChemist]

Bubbling through water is an ideal variant

But methylamine HCl can be dissolved in small volume of water and then this solution added to absolutely alcohol (MeOH, EtOH or IPA) solution of NaOH or KOH (In the equimolar ratio!). And notice, volume of water for dissolve methylamine HCl and water after reaction, must be formed azeotropic solution with alcohol after reaction.