Com ple t e a m ph e t a m in e syn t h e se .

This is everyt hing you need for m aking P2NP, from left t o right :
Pipet t e- aparat us, several pipet t es, dean&st ark t rap, PTFE greas, t oluene, m easuring cylinder
100m l, nit roet hane, benzaldehyde, n- but ylam ine, above t he brown flask a heat ing m ant le and
a 250m l RB- flask.

The rat io s you should use are 1m ol benzaldehyde and 1 m ol nit roet hane and 0,1m ol R- NH2.
Convert ing m ols t o m l s you will find out t hat you will need:
SWI M didn t use 1 m ol right aw ay but first w ant ed t o experim ent wit h sm aller am ount s, so he
used:
17m l benzaldehyde
13,3m l nit roet hane
3,3m l n- but ylam ine
33m l t oluene
Be sure t hat non of t he product s you use will cont ain wat er since when perform ing t he
react ion wat er will evolve which will be t aken out of t he react ion wit h t he dean&st ark t rap
because it prevent s a good yield of P2NP.

All t he chem icals m ixed t oget her.

An overall view
Aft er heat ing it a bit t o get it at 100* C aprox.

A vague pict ure of how it looks like aft er 3 hours of refluxing,

if t he color will get orange t o dark orange before 6 hours you should st op refluxing at t hat
t im e.
But don t reflux it longer t han 6 hours, som et im es you only need 3 hours t hough.
To im prove yield you can also add 1m l of glacial acet ic acid t o buffer t he n- but ylam ine.
For every m ole of benzaldehyde one m ole of wat er will form and since SWI M used 17m l of
benzaldehyde which is ( 17m l x 1,05g/ m l = 17,85g benzaldehyde / 106,12g/ m ol = ) 0,17m ol
benzaldehyde. Thus 0,17 m ol of wat er will form which is ( 0,17 x 18,01 = ) 3,03m l of wat er.
So aft er t he 6 hours or earlier you should have 3,03m l of wat er in your t rap, it will likely be
m ore since your t oluene will cont ain a bit of wat er t oo in SWI MS react ion he got 4m l of wat er.
The color aft er 6 hours of refluxing and collect ing 4m l of wat er in t he t rap.
Now SWI M put s t he round bot t om flask in t he freezer at 18* C because t he P2NP is now
dissolved in t he t oluene but w hen you will m ake t he t oluene very cold t he P2NP w on t dissolve
in t he t oluene anym ore or at least very bad.

7 hours lat er scrat ched t he walls of t he RB flask t o init iat e cryst al form ing.
10 hours lat er a lot of cryst als in t he RB flask,

The crop of cryst als in t he bot t om of t he flask.

Cryst als form ed on t he sides.

Now quickly break up t he m ass wit h a glass st ir rod or a t herm om et er and t hrow t he m ixt ure
t hrew a buchner filt er ( filt rat ion under vacuum ) .
The t oluene will get back t o room t em perat ure and t hus t he cryst als will dissolve back int o t he
t oluene t hat is why you need t o be so quick and necesarilly do need t o use a buchner filt er.
Just a pict ure of t he buchner filt er how it looks like.
Put t he cryst als on a paper t o air- dry.

As you can see t he cryst als are yellow coloured so t hey need purificat ion or else your next
product will be crap and yellow t oo.
The first crop weighed 6,02 gram when com plet ely dry.
The second crop was 8,01gram SWI M evaporat ed off t he half of t he liquid and put it back in
t he fridge.

Evaporat ing off t he half of t he t oluene. Toluene and wat er seperat ed.
Now t he cryst als were purified by dissolving t hem in a m inim al am ount of boiling
isopropylalcohol which is st anding in a hot wat er bat h, when t hey have all dissolved put a
wat ch glass over t he t op of t he erlenm yer and let t hem cool t o room t em perat ure; t hen put
t hem in t he deep freezer and vacuum filt rat e t hem over a buchner filt er and let t hem dry
again.

Beaker wit h I PA st anding in beaker wit h wat er. On t he right t he P2NP cryst als.

P2NP dissolved in boiling I PA. Cooling down, you can see cryst als form ing.

Here you can see t he cryst als form ing while cooling down, in t he buchner filt er t he cryst als
were washed wit h wat er.

From t he 14,03g of P2NP which SWI M st art ed wit h 13,7g of P2NP was left over aft er t he
recryst alizat ion/ purificat ion st ep.
Now it is t im e ( by t he m ean t im e t he P2NP is dry again ; - ) ) t o do t he am inat ed reduct ion of
t he P2NP t o am phet am ine.freebase.

This was first t est ed wit h 3,5g of P2NP:

You will need 5g Al foil cut it int o 1 ( 2,5cm ) squares and t hen fold t hem up t o nugget s and
you should wrap t hem up so t ight t hat you can only st ill press t hem a lit t le wit h your fingers.

This is t he reflux set up t hat SWI M will be using. Close up and m et hanol added which
had 70m g of HgCl 2 dissolved in it .

As sayd above at t he pict ure you will need a solvent like m et hanol and you dissolve HgCl2
inside t he solvent and add it t o t he Alum inium m ake sure t he alum inium is not t oo fine else a
very heavy react ion will occur wit h t he possibilt y t hat m ercury and hydrochloric acid, boiling
m et hanol and hot alum inium will cover you like a vulcano.
The HgCl2 can also be subst it ut ed by ot her Hg salt s like Hg( NO3 ) 2 .
Aft er 10m in average t he Al will st art t o evolve hydrogen gas, depending on t hickness of t he
foil.
I f you use t hin foil wrap it up 3- 4 layers before cut ing squares out of it else it will react t oo
heavily.

The m et hanol will becom e gray/ blue, and t he alum inium will becom e less shiny.

On for hand you should m ake a solut ion of your P2NP t hat will be added t o t he m ixt ure lat er
on.
The solvent used was isopropylalcohol and glacial acet ic acid, in a rat io:
40m l I PA; 60m l GAA; 3,5g P2NP.

You m ight need t o heat it up because t he P2NP will not dissolve easily at room t em perat ure.
The react ion will heat up and when t here are dark spot s on t he Al and t here is hydrogen gas
bubbling of it you can add all t he P2NP solut ion at once t o t he Al+ MeOH+ HgCl 2 .

A lit t le lat er in t he progress, t he m ixt ure get s darker and heat s up even m ore t o a m ild reflux.
By now t he m ixt ure is dark and t he alum inium is dissolving slowely, you can not ice sm all shiny
pieces of alum inium float ing around, ext ra heat is applied here because t he Al was so big t hat
it react ed not fast enough, but hey bet t er slow react ion t han a volcano, right .

Now when alm ost all t he Al has dissolved add 200m l of cold wat er t o t he m ixt ure t o cool it
down.
Then basify it t o pH 12 wit h 50g of NaOH dissolved in 150m l wat er.
All t he rem aining Al will now react wit h t he NaOH and form hydrogen gas and t he m ixt ure will
heat up but not t o a boil, t hat wouldn t m at t er t hough.
Aft er an hour st irring t here had been som e foam and aft er an hour of st irring t he m ixt ure was
st ill quit e hot and all t he Al dissolved now
Tim e t o ext ract your product .
SWI M used et her since it has a very low boiling point so t hat com es in handy lat er on in t he
progress.

SWI M doesn t own a huge seperat ory funnel so he put t he m ixt ure in t he seperat ory funnel in
port ions and added 30m l et her at a t im e aprox. and t he et her is t he upper clear layer ( your
am phet am ine.freebase is dissolved in t he et her now) .
Aft er all t he washed t his was collect ed in t ot al. Anhydrous m agnesium sulfat e was added t o
suck up t he wat er in t heir m olecules and t hus drying t he et her and your product .

Now you only have t o wait 12 hours t o let t he MgSO4 do it s w ork, filt rat e it and t hen you can
let t he et her evaporat e off at room t em perat ure or wit h t he help of a warm lam p.
NOT AN OPEN FLAME! ! !
Et her is very inflam m able.

All t he et her was evaporat ed off and 50m l anhydrous I PA was added t o t he
am phet am ine.freebase.
Then t o anhydrous I PA 98% sulfuric acid was added calculat e how m any m ol am phet am ine
freebase you ve got and t hen t ake 90% of t hat and calculat e how m any m ols of H2SO4 t hat
represent s and add t hat t o 15m l of anhydrous I PA.
Now drip H2SO4+ I PA m ix int o t he freebase which is dissolved in t he I PA.
Here you can see t he cryst als form ing aft er a few drops have been added.
Glass full of cryst als.
I t w asn t t hat m uch t hough but it looks like it is full of cryst als.

Filt rat e it .

And finally pure am phet am ine sulfat e has been obt ained t his was around 180m g.
When only st art ing wit h 3,5g P2NP, when you loose 1g in t he filt er t hat is a lot , wit h bigger
am ount s yields are bet t er anyway.