Síntese de P2P a partir de P2NP

K-Cyanide

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Não, absolutamente no sentido de que a reação não funcionará usando P2P não destilado, não é mesmo?
Entretanto, o produto final é sempre de melhor qualidade quando você usa compostos destilados. E não se esqueça de que o P2P sujo prejudica o rendimento, sem dúvida. É um trabalho tedioso, mas vale a pena.
 

Multivitamin

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Você acha que é absolutamente necessário medir a pressão no sistema ao destilar a vácuo o óleo p2p/óleo de base livre de metano? Ou posso simplesmente conectar a bomba de vácuo ao adaptador de vácuo no novo frasco receptor vazio quando o DCM tiver sido destilado (porque o DCM com baixo ponto de ebulição de 50c destilaria mesmo sem vácuo), ligar o vácuo, aumentar a temperatura até ver os primeiros sinais de óleo p2p chegando ao frasco receptor e manter a temperatura até a destilação terminar?

Estou perdendo alguma coisa? Tenho que medir a pressão do vácuo ou posso simplesmente aumentar lentamente o aquecimento até ver o óleo chegando ao frasco receptor?
 

waltjr5858

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Be careful your pump doesn't suck in your product. If you have leaks anywhere it causes air to flow through the system towards the pump instead of holding vacuum. Causes some product to go bye....
 

Czeczeczecze

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Não consigo obter h2o2 na concentração de 30%. Posso usar 12% em maior quantidade? ou o que posso usar em vez de h2o2?
 

Arakava

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In the video says add hcl until ph 4 - 5 even less.
But in here Says ph 7 - 6.5
Which one is right?
 

GhostChemist

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In general pH should be lower than 7
Acid is needed to destroy residual NaBH4 and for dissolution K2CO3
 

Jack

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@ghostchemist.8647 @GhostChemist I would appreciate it if a demonstration was done on how you would siphon liquid with the use of a vacuum pump, it is unclear how that technique is done? Can you link to the technology which achieves that effect? Is it a add on to a pump?
 

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Jack

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Do you use Hydrogen peroxide and Hydrobromic acid to make bromine in situ because you don't want to deal with Element bromine in a dropping funnel? Can you link to a piece of equipment you use to siphon liquids. A photograph of it? Do you just use a jar?
 

GhostChemist

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In this synthesis that is show in this topic bromine and its compounds are not used. This topic dedicated p2p synthesis from p2np.
 

Jordan Belfort

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What reaction would you suggest to make a onepot (can be barbier-alike) P2NP to P2P which runs at elevated temperature's or room temp.
Iron and aqeous HCL requires refluxing, it's possible at ibc tote but if leak occurs it's finished.

This isn't scaleable to IBC tote. Using other reductant can overreduce (F.E. magnesium in methanol).
 

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Scalable and control reactions for produce P2P from P2NP is the process with NaBH4

Other method from using glycidates (without P2NP)
 

nokospp

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i just perform this synth and failed in h2o2 addition
for anyone trying this method you should try to make it as cold as possible during h2o2 + k2co3 addition if you didnt have patient and poring h2o2 way to fast it will burst out
 
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