Author Topic: oxycodone > oxymorphone  (Read 2947 times)

0 Members and 1 Guest are viewing this topic.

BieneMaya

  • Guest
oxycodone > oxymorphone
« on: November 11, 2003, 04:53:00 PM »
Has anyone tried Epikur´s synth yet?

https://www.thevespiary.org/rhodium/Rhodium/chemistry/oxymorphone.html



Well I found out now, that dope_amine who did
the write up of codeine > oxycodone

https://www.thevespiary.org/rhodium/Rhodium/chemistry/oxycodone2.html


has recognized an error in that synth from epikur.

Ok here´s what he wrote one and half year before
after someone had asked for the critical step Epikur left out:
"    Dope_Amine
(Hive Bee)
02-11-02 04:26
No 267917
         Re: Oxycodone synth   Bookmark    

It's honestly really simple.  Everything is fine with the oxycodone synth like I posted above, but Epikur says to
 add the methionine and everything else and then heat it.  Well, I did this and the reaction didn't work so
I went and looked up the original article (what I should have done to begin with) and the article said that you
heat the solution with everything except the methionine to 40 and THEN the methionine is added.
 I haven't gotten a chance to go at it again cuz the last codiene I turned into morphine (BBr3) and then acetylated it
 (yum) to the purest dope I've ever done.  But that should do da tricky.

Here´s the link for that topic.

Post 241318 (missing)

(taig: "Oxycodone synth", Chemistry Discourse)

Rhodium

  • Guest
Anyone know the ref for the "original...
« Reply #1 on: November 11, 2003, 05:23:00 PM »
Anyone know the ref for the "original article", as well as the link to the post at poppies.org which d_a's text refers to?

merbst

  • Guest
BBr3 demethylation of opioids
« Reply #2 on: November 11, 2003, 10:38:00 PM »

http://www.poppies.org/cgi-bin/forum/forum.cgi?az=show_thread&om=144&forum=DCForumID16


Patent WO8000841


Damn I shouldnt read the hive at work, took me 30 minutes to find that ;-)

Rhodium

  • Guest
Methionine demethylation
« Reply #3 on: November 11, 2003, 10:56:00 PM »
Thank you for that, anyone got the Methionine demethylation article too? That World Patent only referred to BBr3 demethylation of opioids.

BieneMaya

  • Guest
The only one I´ve found is d_p`s original post
« Reply #4 on: November 12, 2003, 04:53:00 PM »
The only one I´ve found is d_p`s original post at poppies.org

http://www.poppies.org/forum/DCForumID16/167_2.html



But there is only one newer post about the oxymorphone synth which tells nothing new.
I searched the actual and archived poppies.org`s opiat chemistry forums.

It would be great if dope_amine would come to the hive again and clarify this matter.
His last access was in spring 2003 so he must be still alive.... :)
Hey rhod- can`t you send him an e-mail?

Rhodium

  • Guest
d_a's addendum
« Reply #5 on: November 12, 2003, 05:05:00 PM »
I just noticed that I already had d_a's addendum on my page, right after the writeup he was referring to:

https://www.thevespiary.org/rhodium/Rhodium/chemistry/oxycodone2.html


Rhodium

  • Guest
Oxymorphone from Oxycodone with BBr3
« Reply #6 on: November 12, 2003, 08:40:00 PM »
And here is a more easily read version of the above WO patent:

https://www.thevespiary.org/rhodium/Rhodium/chemistry/oxymorphone.bbr3.html


hellman

  • Guest
BBr3 and Bcl3
« Reply #7 on: November 13, 2003, 01:20:00 AM »
Boron tribromide is readily replaceable with it's little sister Bcl3, with from what reports from senior pioneers here, the yield is very similar, when exchanging the two,.

Boron Tribromide is very heavily watched
Boron Trichloride is very easily accesible from all good --- suppliers, as it is used from ---s-a welding,!!!

goodluck all,

They're are so many analogues that can be made,
It is truly scary,
Even refluxing Di-acetyl Moprphine, with simple acids branches out alot of multi acetyl derivitives,

You can go from codeine-morphine----di-acetyl---6MAM, and more,


You can pick up 2.5 kg of Bcl3 for around 350$US

hm ;)