I think the key is to do it in small amounts and aquire your reagents slowly.

this way if you do get caught its only on one batch of 50 or so pills and looks more
credable that you are not useing it for synthesis.

if go the whole wack in one go then I think your asking for it.

you'd be suprized what gets through customs especially this time of year.
i've personally orderd several hundred pills in one order i never had a package snagged by customs i think you are a litlle too paranoid.

I killed my dog for being a dog
ye my cat was working for the DEA too smart little fucker.
and it still wanted to be fed when I found out.

this thread is starting to border on hillarity!

Heisenberg: don't push this thread backward with doubt and complaining about the difficulty of getting lysergic amides.

As German said, You can isolate LSA From HBWR cheaply. Also ergotamine tartrate can be bought online as Jon said.

JohnSanders: I am very sorry to hear of you loosing money on bad vendors. Please don't loose hope in making LSD. I beleive that
we need people out there to generate this kind of energy. LSD is a high frequency, high precision biogenetic tool - and we can
really help people with it.

Here's some pointers which I beleive will make it easier for you to get to end result:

1) Hydrazine can be made from urea and sodium hypochlorite (bleach)
2) LSA Can be isolated with chromatography, but you'll need a column.
4) Diethylamine from DEET insect spray by distillation.
5) LSA can be modified into LSD by reaction of the hydro salt with diethylamine.
6) The reaction takes place at 0*C in low-light environment
(in a freezer) and is anhydrous. (you might need some MgSO4)

don't give up hope!

Curse the bastard who ripped you off for paspaltic acid,
and praise you sir, for having the balls to order some of that stuff! (ITS HOT)

If a few of us put our brains together we can figure it out, OR we allready know
how to do this!

PM me and we can discuss this further!

if I were to think of making LSx I would think about HBWR and start looking into getting realy realy nice gear for growing
and doing rotavap and chormatography.

truly too damb easy realy buy the stuff is just a bandaid wiating to be torn off.

I worked it out that you get the same amount of acid per gram of HBWR as you would perpurea as ergotamine has
a lot of waisted weight when you cut the excess molecule off the LSA

only prob then is how ya goen to get your LSA pure enough to get the reactions to work.

also dont make hydrazine with hypochlorite use TCCA.

look into alkoxides for making this anhydrous and you wont get the chirality all screwed up.

check the diff betweed reaction times in alc over pure curtius reactions

dont make your ethyl amine from DEET do it the origonal way with bromoethane just
make sure you fraction your stuff with a nice long collumn.

nitrite can be made many ways just remeber that dry is the rule of thumb.

and the reaction that say dont use inert gass  use it anyway.

red light red light red light damb it when can I fucking go.

bang fucking tree what yo doen in the middle of the road oh I must
be in the uk singing with the merry men now were is that litte fat man
I want a drink for me cat now.

damb it why give it away any one who does fucking 3 years uni will work it out
 in time for fucks sakes earn it for once.

The only viable way of getting a LSD precursor would be to purchase it. You best chance would be a shady foreign pharmaceutical supplier.

This might help? Download Psychedelic Shamanism.pdf from ebooks here http://wizardx.4shared.com Read chapter 8.

my grandfather drank fosters jon

I hate the stuff prefure carlton or dutch beer.

Here is a relatively recent lysergic acid total synthesis which I found. I couldn't find it mentioned on the forum so I'll post it. Hope it helps someone!

Total Synthesis of (±)-Lysergic Acid, Lysergol, and Isolysergol by Palladium-Catalyzed Domino Cyclization of Amino Allenes Bearing a Bromoindolyl Group

Shinsuke Inuki, Shinya Oishi, Nobutaka Fujii* and Hiroaki Ohno*
Graduate School of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto 606-8501, Japan
Org. Lett., 2008, 10 (22), pp 5239–5242
DOI: 10.1021/ol8022648