Author Topic: Hot or Cold?  (Read 2264 times)

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mtnfrogger198

  • Guest
Hot or Cold?
« on: March 20, 2003, 11:56:00 PM »
For anyone who has succesfully synthesized MDMA via the Al/Hg/Nitro method...

Is it better to do it with or without external cooling?

hCiLdOdUeDn

  • Guest
With cooling defintely.
« Reply #1 on: March 21, 2003, 01:04:00 AM »
With cooling defintely. Never do a reaction without cooling because the reaction can literally explode. Boiling methanol/ketone mixture is not healthy to breath. Its good for the reaction to be hot but not out of control. Just keep practicing you will get there. . . ;)


mtnfrogger198

  • Guest
Just Chillin...
« Reply #2 on: March 21, 2003, 01:12:00 AM »
Yeah, that's what I thought. I did it with my precious reflux condenser tube, so not a single vapor escaped.

I was just worried that I let it get too hot, burning up my product. Next time, I'm gonna try a water bath, but not ice water.

hCiLdOdUeDn

  • Guest
You cant really "burn" up your ...
« Reply #3 on: March 21, 2003, 05:42:00 AM »
You cant really "burn" up your product because the methanol would have to boil away first.

I am positive you can get back your mdp2p after extraction and re-distilling.


Rhodium

  • Guest
No, any MDP2P which didn't form MDMA must have
« Reply #4 on: March 21, 2003, 11:00:00 PM »
No, any MDP2P which didn't form MDMA must have been reduced to MDP2Pol.

hCiLdOdUeDn

  • Guest
Fuck
« Reply #5 on: March 21, 2003, 11:03:00 PM »
This explains why swim gets lower yields on the second amination after trying to extract MDP2P from a "failed" amination. Fuck Fuck Fuck. Only if I had known this earlier. Thanks rhodium again.


goiterjoe

  • Guest
reduction of glycol by Al/Hg
« Reply #6 on: March 22, 2003, 08:35:00 AM »
if the glycol was to be mistakenly used in a reductive amination run, would it most likely be first converted to the epoxide and then reduced to the alcohol as well?  Would it most likely form as MDP1Pol instead of as MDP2Pol?

On a tangent thought, if this alcohol were to be attacked by anhydrous HCl gas such as if it were dissolved in Toluene during gassing, would it be very likely that it might react with the HCl to form that red "oiling out" product that has been commonly described here by people who didn't reflux their epoxide/glycol in sulfuric acid long enough?  I think the sulfuric acid reflux reaction is one of the most commonly messed up reactions among many chemists here.  The only writeup I have gotten to work consistently is the one in Shulgin #109, and many people here have claimed he used twice as much as he needed.  Sometimes other people's advice can be dishearteningly expensive.


Rhodium

  • Guest
If the glycol was subjected to an Al/Hg ...
« Reply #7 on: March 22, 2003, 08:36:00 PM »
If the glycol was subjected to an Al/Hg reaction, it would likely remain unchanged afterwards and be removed in the A/B.

goiterjoe

  • Guest
glycol to epoxide formation
« Reply #8 on: March 22, 2003, 09:22:00 PM »
would the glycol be converted to the epoxide when exposed to heavy basic conditions during the A/B process?


Rhodium

  • Guest
Probably not to any greater extent during such
« Reply #9 on: March 23, 2003, 08:08:00 PM »
Probably not to any greater extent during such a short duration around room temp.