Rozdzielanie izomerów metamfetaminy za pomocą kwasu winowego

[Osmosis Vanderwaal]

@G.Patton Mam kilka problemów z tym procesem i mam nadzieję, że będziesz w stanie mi je wyjaśnić.
Nie ma wzmianki o D-met-D-winianu lub l-met-l-winianu. Są to optycznie czynne stereoizomery i nie widziałem żadnych dowodów ani mechanizmów sugerujących, że one nie powstają. Będąc optycznie aktywnymi stereoizomerami, krystalizowałyby one w wyższej temperaturze (tj. wcześniej) niż te nieaktywne. Kolejność byłaby następująca: D,D; L,L; D,L; L,D.
Dlaczego NIE byłoby bardziej opłacalne i wydajne użycie TYLKO kwasu l-winowego, naturalnie występujących izomerów, i usunięcie kryształów l-metalu z rm przed zatężeniem i krystalizacją?

 

[G.Patton]

Wynika to z przeszkód przestrzennych. Nie można ich tworzyć. Jest to opisane w literaturze z innymi przykładami amin. Poszukaj, jeśli jesteś zainteresowany.

Możesz, to zależy od ciebie. Wynik będzie taki sam.

 

[EveryoneHatesCris]

Okay?

 

[Osmosis Vanderwaal]

@G.Patton I find it interesting that you are reacting ammonium chloride with sulfuric acid to make your HCL gas in this write up. I've never before heard of using that method but it is viable. Is there a reason that is preffered over the more common mixtures?

 

[G.Patton]

No difference, It's up you your local reagent availability.

 

[Osmosis Vanderwaal]

I like that there is no water to gunk up the works, like there is dehydrating HCL with H2So4. I think I'll adot this method andski the drying tube

 

[G.Patton]

It's easy to get rid of water by means of CaCl2 tube filter.

 

[Osmosis Vanderwaal]

sure, or a cold trap with H2So4 inline with the output, but if I skip that I can just have a flask, a claison adaptor with a pressure equalizing drop funnel and a hose adaptor on the side arm. 4 pieces of glass, only the drop funnel being extra from a basic distillation set

 

[prvnc]

The tartaric acid method works by selectively crystallizing d-methamphetamine as the l-tartrate salt. Control pH carefully during freebase conversion and HCl gas saturation. Hot filtration and recrystallization in ethanol boost purity but reduce yield (~30% loss normal). Always verify purity with Simon’s test. Exact tartaric acid ratios and repeat crystallizations improve results.

 

[Osmosis Vanderwaal]

theres a rule that says "a good chmist is an accurate chemist" Tartaric acid doesn't "selectively crystallise" anything. that misleading Also d-meth-l tartrate mixes more than one convention of chirality, considering
d-meth=L-Meth=R=meth=legal, and
l-meth=D-meth=S-meth=illegal

 

[FlyMcgee]

Hi, wondering if someone could shed some light on a question, I have. If someone where to follow the video on how to make the Ephedrine synthesis then do the red P/I2/Ephedrine synth could they then use that mother liquor on this d-Meth synth and obtain d-Meth? (Ice)
Cheers

 

[SoldadoDeDrogas]

It would not be necessary because when you are using ephedrine or pseudo as the starting material, the result is always pure d-isomer meth after reduction. It is when we are using P2P or another material that produces a racemic product that we are able to precipitate one of the isomers for extraction, if we choose. While leaving the other in solution.

 

[FlyMcgee]

Thanks for the info.
Another thing, what is “speed”? You know the old stuff that use to be around where it’d make you party all night. Not “ice” and wasn’t so crazy it would make you see shadow people out your window. Usually would come wet and we called it Gas or speed.

 

[SoldadoDeDrogas]

Depends who you are talking to, I guess. I usually demand for the name of a drug or chemical when people say 'it's crank or speed' or whatever.
Speed usually refering to amphetamine.. adderall, ritalin, etc. Particularly home made amphetamine.
Crank is meth that hasn't been recrystallized into ice. It looks like cocaine, white fluffy powder but it is meth.
I haven't been able to get any decent ice anywere so we resolved to DIY

 

[FlyMcgee]

Ok cheers, ok so I’ve been reading the comments on Ephedrine synthesis and they are saying you won’t get D-meth from it doing the Red p- iodine synthesis. Something about racemic and isomers ect. Can someone like G.patton please explain this to me. All I’m asking is if I follow the videos of ephedrine synthesis and the D-meth synthesis will that work or will it be a waste of time/money? Thanks heaps