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dormouse
(Member)
04-23-00
05:18
No
108759
11-Mar-15
Ranter
unregistered posted 07-22-99 07:46 PM
-------------------------------------------------------------------------------hellman, impressive.
made me wonder whether or not 100% acetone substituted for 100% IPA might not improve the process even further by
not interfering with the oxidation process, though.
Methyl Man
Member posted 08-01-99 11:55 AM
-------------------------------------------------------------------------------Hellman, come on back now, this is unresolved. Those who dig the benzo wacker could really benefit from this info.
Are you saying that one can substitute either IPA [i]or[i/] xylene instead of DMF, or are you saying one can use a
mixture of those two in some proportion (please give the ration if it's the latter).
thanks brother bee
Penis Seinfeld
Member posted 08-01-99 01:25 PM
-------------------------------------------------------------------------------WHAT THE FUCK!!!! That is not me up there!!!
Why the hell would you want to impersonate me?
PS
<GRUMBLE, GRUMBLE>
http://chemistry.mdma.ch/hiveboard/novel/000108759.html
1/5
11-Mar-15
rev drone
Member posted 08-01-99 07:38 PM
-------------------------------------------------------------------------------Um, well... This isn't as novel as it gets, actually.
The Wacker oxidation has been done many times in MeOH, EtOH, iPrOH, DMF, DMSO, etc. As for alcohols interefering,
this isn't much of a problem. Yes, Pd2+ species can catalyze alcohol oxidation, but not significantly under the conditions
you're likely to encounter when oxidizing olefins. For that matter, they catalyze the Bayer-Villiger RxN, if you let them,
but to date, that hasn't been a problem.
Barring olefins or amines from usage as solvents, the only practical limitations here really regarding solvent choice is the
solvent's ability to dissolve both the catalyst(s) and reagents. Fer crissakes, using a PTC and the right ligands on
palladium, you can actually even get away with even less than THAT -- by dissolving the olefin and PdCl2 in something
like DCM, and adding an aqueous layer of H2O2, then a PTC to shuttle the oxidizing species from the aqueous phase into
the organic phase, you can successfully perform the Wacker in an ultra-clean cutting-edge way (ref's available upon
request.)
No yields, reaction time, conditions, concentrations, general observations, or even molar proportions with your report?
No mention of the solubility of your catalysts in your solvents system, or the actual proportions of the two solvents, for
that matter? You didn't even tell us what catalyst or catalysts you used. Hmmm. Well, I guess its the thought that
counts. Sorry to be such a party-pooper, but you haven't actually told us anything. I don't mean to sound harsh, but I
feel you have the potential to do some amazing practical research. This still could be handy, provided you were kind
enough to supply more complete details.
Patiently awaiting useable details,
------------------the good reverend drone
Slappy
Moderator posted 08-01-99 09:45 PM
-------------------------------------------------------------------------------Drone:
Actually, what I am thinking, is that if we work on it, we can have a cheap, high yielding, practical Wacker. What about
using another metal besides Pd? I know that Pd is the perfect catalyst for this, but what about a mixed catalyst? Cu
with something else?
How about this. Olefin and catalyst in a cheap organic solvent, H2O2 as Oxygen source, and a PTC to cover the
aqueous -> organic phase transfer.
Even if this does not have the best yield, have you seen PdCl2 prices these days? We can use allot of catalyst (cheap)
and run it for a long time. A traditional Wacker, with PdCl2, CuCl2, and O2, cost a fair amount to run. Especially in large
amounts. A 20L reaction (~1000g olefin) would cost well over $1000.
Hopefully, we can work out a procedure that will be as cheap as making coffee.
hellman
Member posted 08-01-99 10:38 PM
-------------------------------------------------------------------------------Droney ol boy,Methyl MAn
I've told you everything...
If your having trouble solvating your batch with the corresponding new solvent at the SAME qauntity as DMF, Isolate
each component and solvate that seperatly, once everything is solvated
then proceed as normal, Don't look too much into solvents, as long as everything dissolves, keep tabs on the required
amounts of DMF that would have been used, keeping your new solvent, around that mark in quantity, Obviously if you
use 30L of IPA for 100ml safrole, it will take longer, and require, more than likely a much needed huski cap to be truly
fucked(husky hat=one of the hats with the flaps that go over the ears, with the fur).
I'll be back
hellman
Methyl man- No, use either solvents, not both together, although, it really woudn't matter
hellman
Member posted 08-01-99 11:01 PM
-------------------------------------------------------------------------------I'm sorry about the flavour of my last post,,.I'm just in a hurry today,.
Just do the benzo, how strike wrote it,
Just replace the DMF purely with 100% IPA, Xylene, in molar respects.
You will be happy,.
If you have some other solvent, say meoh, impress yourself and disslove it in that,
Small increments in time and heat will dissolve it,.
hellman,
If your really lazy, use meoh as the DMF replacement,Don't even try to dissolve anything and shake the bastard for 4-5
hours, while you watch Dawson;s creek,.
It really all boils down to technique vs yield, have some fun
Osmium
Member posted 08-02-99 04:23 AM
-------------------------------------------------------------------------------http://chemistry.mdma.ch/hiveboard/novel/000108759.html
2/5
11-Mar-15
Slappy:
Processing 1000g of olefin with the O2/MeOH wacker uses about 10g of PdCl2, 4-5L MeoH, ~40-50g CuCl2, plus some
oxygen. Unless you buy the PdCl2 and the other chems from Aldrich, the whole reaction will most likely cost you
somewhere around 200-250$ for the chemicals, not 1000$.
Slappy
Moderator posted 08-02-99 06:16 AM
-------------------------------------------------------------------------------Os:
Sorry bout that, my off the cuff calculations were a little off. It should be 4000g of olefin, in 20L solvent.
Methyl Man
Member posted 08-02-99 10:19 AM
-------------------------------------------------------------------------------Hellman: thanks for clarifying that, you know what a neurotic I am for getting things clear before I jump in. This is nice
because to know because I would rather not buy DMF also, plus I can get 100% IPA for like $6/gallon. Yeeha.
thanks again
MM
anonymous
Member posted 08-02-99 01:05 PM
-------------------------------------------------------------------------------So if I understand correctlly one would only use 100% IPA. Not IPA _and_ xylene. So its a single solvent matrix not a
mixed one.
anonymous
Methyl Man
Member posted 08-02-99 04:24 PM
-------------------------------------------------------------------------------Yes, 100% IPA as in anhydrous IPA (not 100% IPA as in not mixed with xylene). He's saying figure out the molar
equivalent amount of either IPA or xylene as compared to the DMF amount, and use one or the other. Both are really
cheap and OTC for me (thank Buddha).
Now if someone would only post the relative molar amounts (yeah that's right this punk Methyl hasn't learned to
compute that yet). DMF is a helluva solvent, melts the ink on labels instantly, so I'm guessin' that the IPA amount would
be about 130% of the DMF amount.
ymir
Member posted 08-02-99 05:11 PM
-------------------------------------------------------------------------------Osmium: Approximately how much oxygen is requried in the aforementioned procedure?
rev drone
Member posted 08-02-99 07:46 PM
-------------------------------------------------------------------------------Slappy,
There are plenty of metal catalysts for epoxidizng olefins, but only one PRACTICAL one that'll consistantly give you the
alpha-methyl-ketone. If you're willing to settle for that, then the worlds your oyster.
I've wondered, if you sued something like a cobalt, titanium, or nickel complex to catalyze the odixation to the epoxide,
and coupled it with LiBr or equiv. catalyst to isomerize, would this work? There may be some contentions of competing
sulubilities between the catalysts, but it looks kinda interesting.
Hellman,
Glad to see you didn't take me the wrong way. Solubility can be helped by 1: crushing things exta-fine, 2) sonication.
What was your yield? Keep fightin' the good fight!
------------------the good reverend drone
Osmium
Member posted 08-03-99 12:02 PM
-------------------------------------------------------------------------------If I remember correctly, every mole of alkene needs half a mole of O2. 4000g alkene are roughly 25 moles, so about 13
moles of O2 (~400g), plus some loss because of pressure release etc. That's all estimated, don't take the amounts too
literally. Even a small welding O2 cylinder will go a long way for sub-industrial bees.
Methyl Man
Member posted 08-04-99 01:16 PM
-------------------------------------------------------------------------------Anyone wanna toss Methyl a bone and outline the math it takes to figure out the molar equivalents of IPA and xylene
relative to DMF? I mean I know that the math will be handy for figuring out molar stuff on every substance, and I know
Methyl will have to check MSDSs or other sources to get the molecular weights of things, but an overview of how to do
it would be helpful.
Math is not Methyl's strong point (somewhat of a handicap for an aspiring khemist), but he perseveres anyway.
Calculators rule!
Thanks beez
Felonious Monk
http://chemistry.mdma.ch/hiveboard/novel/000108759.html
3/5
11-Mar-15
Osmium
Member posted 08-05-99 03:28 AM
http://chemistry.mdma.ch/hiveboard/novel/000108759.html
4/5
11-Mar-15
-------------------------------------------------------------------------------Since these are only solvents, the molar amounts are not important. No need to start calculating molars for solvents!
Use the same amount of each. If the procedure says 388ml, substitute it with 388ml of the other solvent. Or use round
figures. That's the way I always do it. Substitute with 400ml.
ketone
Member posted 08-05-99 11:30 PM
-------------------------------------------------------------------------------Osmium is right...these are solvents and by their very nature they're just there to allow the molecules of the other
substances to flow around and touch each other.
MeOH, EtOH, IPA will all work just fine. The reason DMF was quoted is because various papers use DMF <I>because it
used to be an extremely popular organic solvent in the lab!</I> Real labs back in the old days wouldn't have had the
supply problems that bees hypothetically have.
-k
Methyl Man
Member posted 08-06-99 01:22 AM
-------------------------------------------------------------------------------Well alright then! That's what I wanted to hear. IPA it is then for my imaginary friend. He thinks it smells better than
that stanky DMF anyway.
Anyone else like the smell of the benzo wacker after the stir? Kinda spicy fragrance, is it not? Aromatically complex
(although I don't think it warrants making a men's cologne from it or anything).
Osmium
Member posted 08-06-99 01:46 PM
-------------------------------------------------------------------------------Try acetonitrile, too. Not quite otc either, but probably cheaper. At least for me.
hellman
Member posted 08-08-99 10:11 PM
-------------------------------------------------------------------------------Methyl man,
It's not critical to molarize the solvent system, But that doesn't mean to say it's not the right thing to do,
For me, I like to have those interactions happening at roughly the same rate and energy as strikey bar post.
Just don't forget too much solvent takes longer, to little takes shorter,
How much variance, how fast's your stirrer, what shapoe your pot,( Just kidding, have fun, you can't fail with this
baby..>!)
Well that's why it doesn't hurt to use molar quant.
But as we are all a little rough on the edges, and this is clandestine chem,.
Fuck it and have a good time,
Tell me your results when you're through,
GOOOOOOOOODLUCK
hellman
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