textfiles/drugs/extractlaa.drg

In article <C1JqB4.B3G@news.cso.uiuc.edu>, ewh52488@uxa.cso.uiuc.edu (Edward Warren Hand) writes:
>Does anyone know about the validity of extracting lysergic acid
>from Hawaiian Wood Rose seeds or Morning Glory seeds.  According
>to the Anarchists Cookbook, althought many on this news group
>seem to question the A.C., you can through a simple process.

1.  HBWR and MG seeds don't contain lysergic acid, they contain various
amides of lysergic acid (but not di-ethyl amide).

2.  It can be done.  I wouldn't trust the A.C. method, though.  It purports
to be a method for converting the stuff into LSD, which it is clearly not.
Although LSD is ~100 times as potent as LSAs, the recommended A.C. dosage
_after_ conversion is nearly double the alt.drugs FAQ recommended dosage. 
This indicates it's probably a simple extraction which is 50% efficient.

3.  If your purpose is to ingest LSAs, you might as well eat (or grind and
stick up your butt or chew) the seeds themselves.  If you are going to use
it as an LSD precursor, most chemists recommend ergot instead.  

That said, here's an old article I saved on extraction.

--------------------------- cut here -------------------------------------
EXTRACTION:

The method I use is a general one - I copied it from one
used by some scientists to extract mescaline from peyote, but I
have since seen close variations used on many plants.
This procedure is followed, whenever a plant is studied for its
alkaloids.

A few ingredients and bits of equipment are necessary.
I am a chemist, and have my own chemistry set. I have considered manufacture,
but I find that there are enough interesting things to do just
extracting natural compounds, which is much easier, indeed, possible
in the home.

You will need:
A few flasks, glass containers, etc. of suitable sizes, depending on how
large a volume you are playing with.
A separating funnel is almost essential - this could be tricky to get without
a little effort. If you don't know, it is an inverted conical flask with a
hole at the top to pour stuff in , and a tap at the bottom to let the stuff
out accurately . It is used for separating immiscible layers.
A vacuum filtration apparatus would be very useful; I did have a bodgy one
rigged up myself, but it was always difficult to use. Some kind of still,
though, is pretty important to have, although conceivably for a once off
you could get by without it, if you don't mind breathing in a lot of solvent.

As far as still goes it is to recover solvent, and leave goodness as a
residue at the bottom. I use a bit of quickfit I nicked: a round bottom
flask, short column, thermometer on top, and a small condenser... takes
for ever, but don't expect to follow this procedure in anything under a
day.

Other bits and pieces:
A filtre of some sort is a necessity; preferably a good one, with a vacuum
pump if you are filtring gluggy stuff (cactus is the worst, sticky goo,
e.g., other things like seeds and bark are better). People have been
known to use such devices as coffee filtres, t-shirts, tins with holes
in the bottom (as a filtre press) and so on. Whatever you can scrounge.
A lab buchner funnel, sidearm flask, and venturi pump are ideal.
All this stuff is standard in any chemical lab, regardless of discipline.
(cont'd in part ii)
CTION part ii:

Chemicals necessary:
The paydirt (obviously)
Some solvents: methanol (lots), and a non polar solvent. Some people use
ether - this is dangerous and doesn't dissolve everything. Your best bet
is probably something chlorinated - I use dichloromethane, although
chloroform will do (don't breath too much - it is fun at first, but ends
up making you feel ill). Drycleaning fluid... petrol.... I don't know
what you have access to.
Dichloromethane is good because it is non-toxic, volatile, and a good
solvent. It has a major drawback: separation is often very difficult
once you have placed your gluggy plant muck in there. The shot is to
use large quantities of everything, and be patient.
You will also need an acid (Hydrogen chloride is good)
and a base/alkali (Sodium hydroxide is good - that way, if you stuff up,
you end up synthesizing salt instead of something nasty.)
Also useful: acid/base indicator paper, boiling chips (porcelain grains)
and activated charcoal - see local chemist.

The idea is this:
Most fun compounds (the only exception is maybe THC, and alcohol if you count
that) are basic - they contain nitrogen.
So: in general, if you react them with hydrochloric acid, the form a water
soluble chloride. If you react them with dilute base in the aqueous phase,
they go back to being a base, which is insoluble in water, but soluble in
organic non-polar solvents (like CH2Cl2). So, the theory is, that only
a base will go from water to solvent and back to water etc. when changed
from acidic to basic and back to acidic. This gives you a way of removing
all the other crap which is not alkaloid from a sample. That is the theory.
When I do this, if I can get down to some brown or green sludge that I can
throw down or smoke, I am happy with a good days work. Ideally, you should
end up with lovely white crystals, but I think that would require a lot
of time and effort, and indeed a considerable loss of product in the process.

Procedure:
Get your stuff.
Dry it as much as possible - this makes life easier later on. You will never
get all the water out, but too bad.
Chop it up as fine as possible: a blender comes in handy.
You may wish to chop then dry. A word of caution : try to avoid exposing
your stuff to excessive heat. I dry in low heat oven. Heat and air destroy
good compounds from upwards of 100 degs C. All this bit will depend on
exactly what you are extracting.
Once it is finely divided - powdered if possible, put it in a big container,
and cover it with methanol.
Alternatives to methanol here are ethanol (not as good) and acetone (good
solvent - rips the crap out of anything, but is more reactive - can react
with your actives).

Now, depending on what your stuff is, you have to let the methanol have time
to remove it all. This is best done by leaving in a quiet warm place for
a few days, even up to a week, and shaking it occasionally so it is mixed.
Some papers recommend solvent extraction (soxhlet apparatus) and refluxing
at the boiling point of the methanol (80 degs or so - I can't remember).
I usually just rely on time to get the good stuff out.
When you are ready (early in the morning), filtre the muck, to give you
methanol+dissolved brown gunk, and a residue soaked with methanol.
The residue still contains a lot of good stuff, so soak again for an hour,
and repeat, and do a third time if you are feeling generous (3 is the
magic number in extraction work).
When you are done, there is another thing you can do finally, if desired:
depending on what your stuff is, mix it up with dilute hydrochloric acid,
1M is appropriate. let stand for an hour, then filtre (this may be very
difficult) That will get the last of the alkaloids out of the substrate.
(continued in part iii)
EXTRACTION part iii

You now have a methanol-plant stuff mixture, and a dilute HCL-plant stuff
mixture, if you bothered to do that part.
Evaporate the methanol, to leave a small amount of goo. This will contain
water, a bit of methanol, and all kinds of resins and muck, and if you
are lucky, the alkaloids.
If a very quick and crude extraction was all that was desired, then after
stripping the last of the methanol with vacuum if possible, this residue
could be smoked eaten or whathaveyou. I leave that to your discretion.
However, if a cleaner product is desired, the double layer extraction
will need to be performed.
Combine the evaporated methanol gunge with the hydrochloric acid filtrate
if you have any. If you don't then mix the methanol stuff with an excess
of dilute (1M) HCl. Feel free to filtre again at this point. Anything of
marginal solubility here is no good to you. Get the stuff as clean as
possible. Boiling with activated charcoal is another useful trick for
removing gunge. Just boil it up, and filter off the charcoal for a
cleaner brew.
You should now have an acid aqueous solution of alkaloids and water
solubles from the plant.

Take your acidic solution, and bassify. This is done by mixing in dilute
sodium hydroxide (I use up to 5M to save on total volume. Be careful with
conc NaOH - apart from eating skin, it eats alkaloids) As you mix in the
NaOH, you will see swirls of white precipitate form and redissolve.
Continue until the white swirls stay, and until the solution is quite
cloudy. Indicator paper is necessary to see that the solution is basic.
If you can't get indicator paper, you can make an indicator by boiling
up some purple flowers. The dyes in most flowers go bright red in acid,
and green in strong alkali. Just a drop of dye and a drop of mixture
should tell you what is acid or base.

The white precipitate is the alkaloids. The more the better.
Next, add equal volume of non-polar solvent (dichloromethane) to the mix.
Place in separating funnel, and shake. Separate. This may be very difficult
or slow. Adding more solvent, more basic water, etc. may help. Adding lots
of salt to the water layer will help break an emulsion. Ideally you want it
do this step 3 times - to extract as much as possible from the water layer
into the organic. I find this part very difficult, and you have to accept
that you will lose quite a lot of material here. It is, however probably
easier with some plants that others: cactus is very difficult, barks and
seeds would be easier. Use plenty of salt, and agitate to separate.
When you have finished extraction, chuck the basic water layer.
The solvent layer is kept, and can be backwashed with salty water for a
cleaner mixture.

The solvent can now be dried, (using salt or some dry powder, the filtred)
(I don't usually bother with this - the old hairdryer at the end can
remove some last solvent and water) then strip the solvent in a vacuum
to get your final product - some kind of syrup could be expected.
This is super concentrated, but may only be half the strength of the
original. e.g. put in enough for 10 doses of morning glory seeds, get
back 5 doses or more of concentrated alkaloids.
If it is desired to take the process still further, you can do the obvious
thing - mix your solvent layer with dilute acid again and extract back into
water. Acid layer could be evaporated under vacuum to give salts of
alkaloids. Alternatively, if the organic layer were scrupulously dry,
bases could be salted out with some organic acid - a tartrate, oxalate
could be formed. I have never bothered with such things - you would need
a lot of pure extract to be bothered.
The acid-base extraction process can be continued as many times as is
desired.

If a truly pure product is desired, the only way to go from here is
chromatography. I have never used this at home, and wouldn't think
it was worth the trouble, but there will be papers available on what
was used for a particular extraction case.

J
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Keith Lewis             klewis@mitre.org          "Mr. Cheap"
I don't dance to music; music dances to me.  Email me for my PGP key.
The above may not (yet) represent the opinions of my employer.