CBD > D8/D9 Mechanics (New Paper)

With the vigorous stirring I use in my reactor, and keeping it at 65c, I seen temp increases the faster I spin. That’s what gave me the idea of using a heater/chiller to keep the temp more stable.

As I increased the speed slowly, I would drop the temp on the jacket of the reactor till I was able to achieve the fastest RPM stir and keep it at 65c so I can see some of that being exothermic. Trying like hell to not over shoot by moving slow on raising RPMs and consistently dropping the chiller temp as to not create too much heat from the reaction.

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If you increase the stirring, you slightly speed up reactions. By mechanically increasing convection, the reaction relies less on slower diffusion of the reactant(s) toward the catalyst. Thus it produces more heat.

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Yeah… what you said :joy:

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Anddddd…

I have to run another sample down because the lab boofed it :roll_eyes:

I sent a 1 gram sample down and not my typical 3 (not sure what the hell I was thinking on that one).

I need my own shit :thinking:

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Boofed it you say? Like put it in their south mouth?

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Might as well have.

Hard enough to do this shit, get ready for Christmas, and make sure virtual schooling is running smoothly for the kiddos and take time to run an hour 1 direction to run more shit down there.

After the 1rst of the year, I’m getting my own analytics FFS.

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Finally came in…

Not bad for f***ing off and trying temp swings :man_shrugging:t3:

Now, to sweep it and try the next solvent

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How long did you run this?

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Have to look back at my notes but roughly 2 hours, I believe

I definitely caught some heads in this batch (dumbass was distilling after being up already for 24 hours)… missed the swap.

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This was phosphoric and ethanol?

Weren’t you going for high d9?

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No… I was dialing in D8 to see how close I could get to low D9. I have a tendency to bounce around with shit like this so I wanted to lock in this process before moving to D9.

That’s next and already have (what I feel to be) the perimeters to flip those numbers.

Heptane and pTSA, not dried, and no argon for this run.

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2:1 heptane to disty by weight, 1% ptsa 30 minute reflux under argon

I think running it for longer will reduce the d9

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Don’t use monohydrate :wink: other forms

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Damnit…

You take all of the fun outta experimenting, ya know that?!? :joy:

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This was mono hydrate

I have the sop for anhydride

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Might as well save you some time :wink:

Youre a cool cat, I like helping ppl that deserve it

If you run it for longer lmk the results!

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Dang… I got 90% in heptane once but not in 30 min- seems like it isn’t done until the solution goes to a deep red rust color, like oxidized blood. I find the tines can be all over the place if the temp changes in small increments like 5C

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If we increase the amount of acid in a system like ptsa and toluene/heptane where things are inmiscible. Let’s say we know the minimum amount of acid needed to get a full conversion. What if we raise the amount of acid by factor 10 or 20. What exactly is changed due to the higher amount of acid?
Would this speed up the rxn and if it does, what is the reason for it?

Higher rate of successfull collisions, increase of energy, nothing will change or something else I am not aware of atm?

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Surface are is real

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PTSA anhydride will only make CBD tosylate at C1 and possibly C5, but not catalyse THC formation.