LSD synthesis from lysergic acid via PyBOP
- Thread starter WillD
- Start date
Hi guys, does anyone know about hydrolysis of ergotamine with sodium dithionite and KOH?
This topic seems majorly underrated. It seems downright revolutionary compared to how I learned to make it.
I read an exchange where someone suggested the methyl ester could racemize during hydrolysis. Is this a concern with the entiopure d isomer? I notice TLC is not included in the work up.
Is a rotovap really optional? This method to be approaching bathtub synthesis without it. No heat? This sounds simpler than mdma or amphetamine.
What am I missing here? Do we work under yellow or red light? What are the major complications? Does the final product yeild isolsd at all?
I read an exchange where someone suggested the methyl ester could racemize during hydrolysis. Is this a concern with the entiopure d isomer? I notice TLC is not included in the work up.
Is a rotovap really optional? This method to be approaching bathtub synthesis without it. No heat? This sounds simpler than mdma or amphetamine.
What am I missing here? Do we work under yellow or red light? What are the major complications? Does the final product yeild isolsd at all?
- By Nicoino
Get reasonably pure LA is a pain in the ass, nearly all the hydrolysis lead to brown/black product which as to be purified.
Even with good quality LA the coupling reaction mixture gets brown black and the work up is not as simple as it is stated (maybe if you start with 100% pure precursors, solvents degassed and professional equipment you have a small change of not happening, but for the home chemist dark solution has to be expected).
Purification of the product is no joke if you don't have access to column chromatography or if you don't want to remove liters of solvent under vacuum.
Even with good quality LA the coupling reaction mixture gets brown black and the work up is not as simple as it is stated (maybe if you start with 100% pure precursors, solvents degassed and professional equipment you have a small change of not happening, but for the home chemist dark solution has to be expected).
Purification of the product is no joke if you don't have access to column chromatography or if you don't want to remove liters of solvent under vacuum.
- By PlanckB1
This has been my experience as well, repeated recrystallisations of the lysergic acid from hydrolysis resulting in a powder which becomes lighter brown each time but still not as light/pure as you would expect. Do you recommend column chromatography of the LA or just column chromatography of the final freebase LSD?
- By Nicoino
I don't think it's worth on the LA, probably with a good workup and enough experimentation it's not even need on the final product.
Big acid chemist like pichard used to synth kilos every month, and I really doubt they were able to chromatograph that amount of product, nearly impossible with a factory.
Big acid chemist like pichard used to synth kilos every month, and I really doubt they were able to chromatograph that amount of product, nearly impossible with a factory.
@G.Patton @William Dampier , can sodium hydroxide or potassium hydroxide be used instead?
Is the ammonium hydroxide used to reach certain PH or does it donate an ion?
Does any vendor offer: "ammonium hydroxide (NH4OH) "?
Is the ammonium hydroxide used to reach certain PH or does it donate an ion?
Does any vendor offer: "ammonium hydroxide (NH4OH) "?
Hi @William Dampier thank you for the synthesis route.
I am not a expert, I have only experience on CBD isomerization to d8.
Now I'm trying to figure out whether it's possible for me to make LSD.
My current goals are:
I am not a expert, I have only experience on CBD isomerization to d8.
Now I'm trying to figure out whether it's possible for me to make LSD.
My current goals are:
- Find detailed route from D-Lysergic Acid Methyl Ester
- Obtain all reagents
- Learning safe handling of the reagents
- Learning Thin-layer chromatography
- Learning Column (Flash) Chromatography
- Make LSD
- Recycling and safe disposal of reagents
- You write that we need 0.84 g Diethylamine (cas 109-89-7), is that correct?
- I ask because according to https://www.sigmaaldrich.com/ it is a liquid and I saw it from Chinese sellers sold in kg.
- Which TLC plates are best suited for this synthesis?
- H type does not contain calcined gypsum binder or fluorescent agent.
- G type does not contain fluorescent agent, contains calcined gypsum binder.
- HF254 type contains fluorescent agent, does not contain calcined gypsum binder
- GF254 type contains both calcined gypsum binder and fluorescent agent
- Can you help me with the route from D-Lysergic Acid Methyl Ester?
- By HerrHaber
It so happens that diethylamine is not regulated in some countries and I have access to it, so subgram quantities can be thought of sendable especially in a protected form. Within this particular synthesis I think it can be eluted through GF254.
↑View previous replies…
- By HerrHaber
In this very particular situation the liquid is weighed for precision... volumetrically you need a micropipette to get accurate quantities. Some times precision is decisive in synthesis, also methyl-diethylamine NMe(Et)2 needs to be precise. Large volumes are seldom weighed.... since volume is easier depending on viscosity and reactivity. Honey like stuff is clearly easyer to weigh and reactive liquids may be approached with syringe volume wise but sometimes if the quantity is small it is pipetted in a flask on a scale drop by drop to the needed mass. Under inert athmosphere is tricky and requires schlenk line and equipment ideally a glovebox (schlenk line and all the paraphrenalia like Argon and liquid nitrogen traps), glovebox I fantasized of building one (I actually built a working microscope when I was seven).
Is there an alternative to using a rotovap machine?
- By WillD
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