Síntese de anfetamina em um único recipiente a partir de P2NP com NaBH4/CuCl2 (escala de 1kg)

SelfExper1menter

Don't buy from me
New Member
Joined
Apr 4, 2023
Messages
17
Reaction score
2
Points
3
Olá a todos. Tentei fazer um pouco de anfetamina usando esta receita em pequena escala, mas falhei. Tudo parecia bem, mas depois de secar o meu produto parecia um pó branco com um toque de vermelhidão. Se fosse sulfato de anfetamina (que eu estava a tentar fazer), o rendimento seria de 84%. O problema é que não se trata de anfetamina.

Efeitos fisiológicos
Experimentei 20-30 mg, houve definitivamente estimulação, mas também provocou febre e, aparentemente, uma diminuição da imunidade: das duas vezes que a tomei durante vários dias seguidos, adoeci com infecções respiratórias (da primeira vez pensei que fosse coincidência). Outra pessoa que a tomou não sentiu qualquer estimulação até 90 mg, apenas alguma secura na boca. Nenhum de nós tem tolerância a estimulantes.

Testes químicos
1 g do pó dissolve-se completamente em 10 ml de H2O.
Quando adicionei uma solução de NaOH em excesso a uma massa medida do pó num tubo de ensaio, obtive um volume aproximadamente correto de base livre com cheiro a amoníaco. Separei a camada de base livre, sequei-a com CaCl2 e tentei titulá-la com ácido. Como resultado, medi a massa molar da base livre como sendo cerca de 171 (e para a anfetamina é 135). Embora as minhas medições não tenham sido muito precisas, a diferença é demasiado grande para ser explicada apenas por erros de medição.

Os meus desvios ao procedimento

1) Ao adicionar P2NP, apercebi-me que ia demorar horas, por isso fiquei impaciente e mergulhei o balão de reação num banho de água à temperatura ambiente. Depois disso, consegui adicionar o P2NP quase todo de uma vez, e a temperatura da mistura não ultrapassou 40-50 °С.
2) Eu estava seguindo o vídeo, então eu não evaporei o IPA e adicionei conc. ácido sulfúrico para a camada IPA / freebase diretamente.
3) Eu não tinha acetona no momento, então não a adicionei antes de acidificar e lavei a pasta filtrada de "sulfato de anfetamina" com IPA.
4) O IPA é menos volátil do que a acetona, pelo que tive de colocar o meu precipitado numa estufa durante várias horas para o secar até atingir um peso constante. A temperatura no forno não excedeu 80 ° С.

Então, a grande questão é: onde é que correu mal? Eu não ficaria surpreso com baixo rendimento ou nenhum produto, mas obter um bom rendimento de uma amina que não é anfetamina?
 
View previous replies…

OneTensionSkyRed

Don't buy from me
Resident
Language
🇺🇸
Joined
Dec 24, 2024
Messages
15
Reaction score
4
Points
3
That's what I was thinking. This reaction produces N-OH-amphetamine instead of pure amine. People can clearly tell the difference between their physiological activity.
 

pekonias

Don't buy from me
Resident
Language
🇺🇸
Joined
Jun 26, 2024
Messages
7
Reaction score
4
Points
3
I don't anderstand what is happening? I used 300g NaBH4 2.07 L IPA, 1.03 L dH2O, 173g P2Np 22g CuCl.2H2O and everything went well - reaction over and I add 0.4 L 25% NaOH sol. to get (pH 13.5) separate layers but... there's wery little separation. The aq. layer was only 0.3L so now I have 2.2 L organic layer, more than starting IPA + H2O (2.1 L). So does organic layer now contains NaOH? The pH after reaction was ~12 and there was no layer separation so I added the 0.4 L NaOH sol. What should I do now? Add more NaOH sol. and vacuum distill? Maybe acidify to pH <=3 and distill. Please advice guys.
 

pekonias

Don't buy from me
Resident
Language
🇺🇸
Joined
Jun 26, 2024
Messages
7
Reaction score
4
Points
3
Obviously I can't count, actually got correct volume for the organic part and also extracted the sludge with 0.3L IPA. It's very confusing when told to add NaOH to pH 12 when it's already at that after reaction. Also aq. part seems to small but it's mostly in the black mud. Going to go ahead with water aspirator vacuum distilling off the IPA and hopefully not lose all product like last time. I think got too hot 80C with -28" Hg vacuum last time. Maybe report how it went tomorrow if has any luck.
 

OneTensionSkyRed

Don't buy from me
Resident
Language
🇺🇸
Joined
Dec 24, 2024
Messages
15
Reaction score
4
Points
3
You need to add more NaOH in dry form or at least concentrated NaOH solution if you don't want to heat RM from dry NaOH to separate IPA layer. The densities are similar and that prevents IPA from salting out. Have you destroyed borate adducts afther the reaction?
 

two777

Don't buy from me
Member
Language
🇺🇸
Joined
Oct 27, 2024
Messages
4
Reaction score
0
Points
1
what is the optimal temperature for a-oil, before you start the extraction/ crystallization process using sulfuric acid? Usually im working with room temperature oil, and adding acid gradually, by not extending temperatures above 40c.
 

pekonias

Don't buy from me
Resident
Language
🇺🇸
Joined
Jun 26, 2024
Messages
7
Reaction score
4
Points
3
Follow up to my previous post, copule observations made during the process I think are important to share. This was really my very first success at this. From 173g P2NP I got ~130ml clear oil. What I wanna say is that now, compared to the previous experiment, was very different at the step when CuCl added. Previously added it dropwise and the temperature didn't increase at all, no storm in flask and only gave test subjects a runny nose. Now had twice as much and better quality P2NP. Also 10% of the NaBH4 was added later, after most P2NP had been added but it don't seem make no difference. So the CuCl was added added in 3 bursts of 10ml each and very violent reaction was observed (~1/4 CuCl soln. was left unadded). After each 10ml addition the reaction almost came out of the flask but not quite and the temperature increased dramatically. The Rm was 3.1 L in 5 L RBF. Temp reached 78C after third addition and the surface / foam level stayed really high for a minute and the reflux from the two ball condensers poured down IPA/H2O like hell. Unreal sight but it happened and I think the reflux prevented temp. going > 78C. So I much rather want the violent reaction then I know something is really cooking and reacting. The organic layer was condensed in -26.25" Hg vacuum BP 37-38C. Vacuum dist. stopped when 1.8 / 2.2 L liquid was removed (BP. was 41.8C at end). Then steam distilled. First 100ml of distillate thought to be water and almost thrown away! It's A-Oil! Thinking drying some of it by mixing 50ml Oil with 300ml? dry IPA and giving it 20g silica gel and let sit overnight. How much H2O should the vacuum distilled IPA contain? Would be nice to re-use it. I measured its density to be ~0.8g/ml which is that of IPA (0.786g/ml) within the measurement accuracy?
 

Attachments

  • RZx3oQeIzW.png
    RZx3oQeIzW.png
    538 KB · Views: 14

keras

Don't buy from me
New Member
Language
🇺🇸
Joined
Jan 18, 2025
Messages
1
Reaction score
0
Points
1
So to cook 1kg of amph would cost more than to make 1kg 3cmc?
Becausd borohydride I see costly in poland , also p2np add up. While 3cmc is one main precursor.
And how these guys sell amp paste for less than 1k per kg. Where profit comes from ?
 

dobrytowar55

Don't buy from me
Member
Language
🇵🇱
Joined
Sep 21, 2024
Messages
4
Reaction score
0
Points
1
So then i Ask for most beacuse i knows on netherland production cost is between 300-600euro. How ? I dont mnie but meaby someone tell me herę 😅
 

dobrytowar55

Don't buy from me
Member
Language
🇵🇱
Joined
Sep 21, 2024
Messages
4
Reaction score
0
Points
1
Hi. Can someone tell me what the cost of ingredients and equipment for producing 1kg is? I would be grateful if someone could tell me if it is enough to scaling up everything to get a larger amout or does that cause any discrepancies? Also can someone tell me what is the CAS of this final product?
 
Last edited:

OneTensionSkyRed

Don't buy from me
Resident
Language
🇺🇸
Joined
Dec 24, 2024
Messages
15
Reaction score
4
Points
3
It would be really REALLY great if someone could run a TLC analysis of the products from this reaction. I've read that NaBH4/Cu reduction mainly produces N-hydroxylamines instead of amines for alpha-alkyl nitrostyrenes. Because of similar melting points for their salts and similar boiling points, the only way to separate and identify N-OH-amphetamine is by chromatography. The N-OH product is also active as a stimulant but it is different to amphetamine. I wonder if this is really true.
 

GhostChemist

Expert
Joined
Nov 20, 2022
Messages
199
Reaction score
330
Points
63
what source reports this information?
all compounds tested with qualitative and quantitative analysis
N-OH group can be formed as an intermediate compound if the experiment is not carried out correctly
 

chemdogpal

Don't buy from me
New Member
Language
🇺🇸
Joined
Mar 4, 2025
Messages
6
Reaction score
0
Points
1
at what temperature does amphetamine start to evaporate ?
 
Top