06-24-02 05:26
No 324741
MDP2P / MD Benzene + Acetone cat. Mn(III)
As i read in TFSE 1,4 dimethoxy benzene + acetone catalysed by Mn(III) can be used to obtain MDP2P -Al/Hg/MeNO2-> MDMA!!
so here my question:
can 1,3 dimethoxy benzene also be used ?
Chemistry are not only the things that stink. :)
(Hive Bee)
06-24-02 06:28
No 324754
Probably yes.Differences between of them is that just position of one methoxy group differs a little.It is still attached to benzene ring just to 3 position instead of 4.It shouldn't make much if any difference in reaction.Again i'm not 100% sure so wait for confirm or denial from anybody more experienced.
A friend with speed is a friend indeed
(Official Hive Approximator)
06-24-02 06:40
No 324757
jan: please post the # of the post you found this info in.
neither 1,3-dimethoxy-benzene nor 1,4-dimethoxy-benzene are useful
for making MDP2P. (look at the molecules and try to see how that
should work...)
what 1,4-dimethoxy-benzene might be good for is 2,5-dimethoxy-P2P,
a precursor to the DOx series.
(Old P2P Cook)
06-24-02 06:46
No 324762
As i read in TFSE 1,4 dimethoxy benzene + acetone catalysed by Mn(III) can be used to obtain MDP2P
Wow! That is a pretty neat trick, not only move the location of the phenyl ethers but convert them from methoxys to methylenedioxys as well. This must be something from the Harry Potter School of Chemistry.
so here my question:
can 1,3 dimethoxy benzene also be used ?
1,3 dimethoxybenzene can be used for a lot of things. What is it that you are asking about?
(Newbee)
06-24-02 10:01
No 324809
The heading to your post says MD benzene, but the body says
1,4 dimethoxy benzene. WTF? typo?
(Hive Bee)
06-24-02 19:17
No 324985
You could use said substituted benzenes in a friedel-crafts reaction with 1-chloroacetone. This will yield a lot of side products. Depending on the substituants the side products may be very hard to separate. There must not be any ketone or alcohol groups attached to the benzene. You need about 2.1 moles of catalyst to 1 mole of 1-chloroacetone. The benzene compound must be used in great excess (10 moles or more).
(Hive Bee)
06-24-02 22:48
No 325060
Sorry guys i was to far away from planet that i haden't read what i wrote, so here my corrected question:
can 1,3 diMeO benzene be used make DMA as starting matrial for dob or doi ?
Chemistry are not only the things that stink. :)
(Distinctive Doe)
06-24-02 23:43
No 325077
Looks like your still on a far away planet!
It should bee 1,4
This place might help
http://www.chemfinder.com/
Those who give up essential liberties for temporary safety deserve neither liberty nor safety
(Hive Bee)
06-24-02 23:57
No 325083
i only wanted to know if it is possible to make anything psychoactive out of the 1,3 diMeO benzene. so thanks foxy to get me back to earth
Chemistry are not only the things that stink. :)
(Stranger)
06-25-02 03:55
No 325112
If you'd use 1,3-dimethoxybenzene in the manganese catalyzed acetonylation there will be several products.
Like 2,4-DMP2P, 3,5-DMP2P and 2,6-DMP2P. These may serve as precursors for, let's say 2,4-DMA, 3,5-DMA and 2,6-DMA, but not for the DOB/DOI derivatives.
Using 1,4-dimethoxybenzene only yields 2,5-DMP2P, which of course is a very valuable precursor for the DOB/DOI derivatives.
(Hive Bee)
06-26-02 11:05
No 325698
Palladium can be used to couple a nucleophile to an aromatic ring. It's in a book I have, so I'll check up on it. In basic solution, acetone becomes deprotonated to some extent at the alpha carbons, so it would be a nucleophile. Under the right conditions, this might just work.
(Stranger)
06-26-02 11:20
No 325708
Why would you want to waste valuable Pd on this, when you can acetonylate with a manganese catalyst?
(Hive Bee)
06-27-02 10:44
No 326107
1) It is probably possible to use supported Pd in a heterogeneous reaction. Therefore, it doesn't go to waste.
2) Pd does a better job at just about any catalyzation than anything else.