Complete amphetamine freebase (A-oil) synthesis from P2P(10L scale)

blackburn

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OrgUnikum

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Congratulations!

There seems to be quite some base in the water layer though, if you do not want to extract it you can add about the same amount of brine (saturated salt - NaCl - solution, easily prepared beforehand, this will press base out of the water layer and also suck some water from the base. Ideally the whole water layer would be saturated with salt but I suppose you are in a hurry so adding brine will do. You see the result after 5 to ten minutes, the water layer becoming clearer, but give it half an hour to do its job completely.
 

blackburn

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JFgos6LOqT
 
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OrgUnikum

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Thats also steamdistillation, what you want to say is that you did not use an external steam-source, generator but boiled it from the reaction vessel.
Boiling point of Amphetamine Base would be around 200 °C

It is recommended to refill water in this case so there is always plenty of water around. Amphetamine base will then come with water at 94 to 98 °C measured at the stillhead/Claisen/entry of condenser.

Steamdistillation is contrary to common belief more sped up by having a wide undisturbed path for the steam then by heating like mad.
 

blackburn

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Yes thats what i men, No external steam-source...
 

blackburn

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Yes thats what i men, No external steam-source
 

btcboss2022

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In case of A-oil you need an external steam source in addition to the water in the mixture to obtain the max yield, that's checked many times and always you can test it yourself. Only adding water and distill it won't obtain the max yield.
 

OrgUnikum

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External overheated steam for sure considerably speeds the process up and I do not doubt that there will be more oil in the collection flask in the end. But I am afraid it is not more Amphetamine base but other stuff formed in the reaction. Amphetamine and Methamphetamine both distill with willingly with steam even from a just simmering flask and thats not just my imagination but it is well-documented in the literature.
This is more a point when somebody uses your base-hydrolysis method as when your acid-hydrolysis is used as in the acid hydrolysis you have a washing with DCM step before basification included which removes all non-basic unwanted stuff like leftover P2P, no such step is in the procedure with base.

Look, I want to express my gratitude for you posting this large scale method here, I seriously appreciate it very much and I want to assure you that what I write is intended to be constructive and no attempt to criticize you personally or to ridicule your abilities and achievements.

I do not know if you treat the oil from this reaction in any further ways, workup wise, for higher quality and to remove impurities or if you process it directly to "Paste" and however you do it, I am not here to judge, if your customers are happy they are happy.
For personal consumption I rather steamdistill very gently and then add some more steps but I am very old and got very sensitive to impurities in general.....
 

btcboss2022

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Don't be afraid about this point I can assure you that there is more amphetamine base it's measured after solvent extraction.
In chemistry sometimes (not many) the literature differs a little from the synth reality and this is possibly one of those cases anyway I insist that you can check it yourself without problem and then comment it here.
About the solvent washing is an optional procedure since it will be steam distilled anyway and after distillation no impurities but even if you are afraid of impurities you always can make an acid-base washing when you extract the final freebase with solvent after distillation ;-)
 

KGB

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why is there three layers?the upper layer seems to be the freebase and its seems extremely small and highly doubt 70% yield
 

Davidrobinson

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Is that picture after internal steam distillation?
Did you distill your p2p for 70% yield , or did you use it straight from bmk ?
 

blackburn

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Yes it is .

I used The P2P immediately after conversion from 5449, i did not distill it.
 
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Tweaker

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I tried both hcl and phosphoric. Then nabh4 reduction both times. I'll dm you photos if I can find it
 

tucoXxX

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Hello. Is 37% formamide suitable for synthesis? this is all I found in our country.
 

tucoXxX

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Formamide 75-12-7 is what is needed. Aqueous solution is not good , I think . Does anyone know where I can buy it in Europe? I haven't found it yet
 

OrgUnikum

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Formamide is watched you can make it yourself. Ammonium Carbonate + formic acid = Ammonium formate, heat to 175 °C (to remove water) and hold there for a few hours -> Formamide. Precise temperature control and good ventilation is a must, Formamide starts to decompose at 180 °C. The formic acid is used in a slight molar excess.
 

tucoXxX

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so order carefully, because the authorities are watching. I did not know . thank you very much . I will try to make it ... but it would be better to buy it. Chinese partner wrote $30 / liter, with delivery. is this a good price?
 

OrgUnikum

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I would say its ok if its "secure line" or however they call it, say everything regarding import is taken care of and you are not involved at all and it will be sent to you as EU internal shipment. And its not more then 25 kg. 50 kg should already be cheaper, 100 kg even more etc.
That's just my opinion, absolutely subjective.
 

marapiasss

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Is there any way to know if the A-oil is diluted in something? or its purity?
 

OrgUnikum

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TLC, thin layer chromatography. It is not difficult if one just wants to check for the presence of other compounds, qualitativ. Doing it in a way which allows quantitative estimations (how much of different compounds is there) is demanding though.
 
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