Dextroamphetamine Synthesis (Nabenhauer, 1942)

G.Patton

Expert
Joined
Jul 5, 2021
Messages
2,712
Solutions
3
Reaction score
2,870
Points
113
Deals
1
We took 6g of racemate = 3 g of D-amph+3 g of L-amph
We got
2.63g yield = x%
3.0g theory = 100%

2.63*100/3=87.7%
 

Pororo

See my products
Seller
Language
🇺🇸
Joined
Jan 23, 2024
Messages
110
Reaction score
46
Points
28
Deals
12
Thanks for an interesting study. But I'm surprised with your tartaric acid proportions.
6g of amph sulphate is 3.49 g of racemic amph base. Then why do you use 2.45 g of d-tartaric? It shall come in molar proportions 1:4, i.e. 0.97g of d-tartaric is enough???
 
Last edited:
View previous replies…

Pororo

See my products
Seller
Language
🇺🇸
Joined
Jan 23, 2024
Messages
110
Reaction score
46
Points
28
Deals
12
sorry, I also made a mistake in calculations.
6g of amph sulphate is 4.41 g of racemic amph base. D-tartaric in molar proportions 1:4 is 1.23g as it is the same as suplhate: 1 mole of acid per 2 moles of amph. 2 times less than you count it.
 

G.Patton

Expert
Joined
Jul 5, 2021
Messages
2,712
Solutions
3
Reaction score
2,870
Points
113
Deals
1
Hello, 6g of amph sulphate (368.5 g/mol) contain 0.03256 moles free base (look at the reaction equasion, where 2molecules of amph produce 1molecule of salt and vice versa). Briefly, one mole of sulphate salt contain two moles of free base, hence moles of amph sulphate multiply x2 (0.01628x2).

Your question is why it's written to take 2.45g of d-tartaric acid.
Answer: 2.45g of d-tartataric acid is 0.01632 moles (2.45g/150.09g/mol). Hence, this 0.01632 moles (2.45g) is half of 0.03256 moles of racemic amph free base.
You need 1/2 cuz this racemic amph free base contains 1/2 of d-amph and l-amph in theory.

Do you understand?
 

Pororo

See my products
Seller
Language
🇺🇸
Joined
Jan 23, 2024
Messages
110
Reaction score
46
Points
28
Deals
12
I got your idea. I don't know why you believe you are going to get bitartrate. May be because of ethanol.

If I understand terms correctly, tartrate means 1:2, but bitartrate means 1:1 molar proportions!!!

But I don't use ethanol. I use other solvents.

What I know, crystallization stops as soon as 0.25 moles of acid consumed with yield 95%. Then, if 0.25 moles of opposite acid is added, precipitation will start again with yield 95%.
And now, when 0.25 of L and 0.25 of D were applied, if I try to add more D or L or DL acid to mother liquor - nothing happens. It looks there is no base, ph is also acidic.
For the prove, may be, may be, on occasion. Not sure when I will do amph separation again, end of September may be.
 
Last edited:

Pororo

See my products
Seller
Language
🇺🇸
Joined
Jan 23, 2024
Messages
110
Reaction score
46
Points
28
Deals
12
I think, the point is here mr. Patton, and it is very simple: sequence fucking matters!!!

1. If you have a flask with with 1 mole of tartaric acid, d or l or dl, whatever, and start adding 1 mole of corresponding base in small portions, in the result you will get mostly bitartrate and some tartrate (+ some unreacted acid probably) with salt's resulting PH = 2.
2. This is what I do! If you have a flask with with 1 mole of base and start adding 0.5 mole of tartaric acid in small portions, in the result you will get mostly tartrate and some bitartrate (+ some unreacted acid.) with salt's resulting PH = 5.0-5.5.
Or 1 mole of racemic base and 0.25 mole of d or l acid if you are targeting to separate them
 
Last edited:

JoshL1221

Don't buy from me
Member
Language
🇪🇸
Joined
Sep 3, 2023
Messages
3
Reaction score
0
Points
1
hi, excuse me, when you say "We precipitate d-amphetamine with an additional amount of d-tartaric acid.", how much d-tartaric acid is used? thanks.
 

G.Patton

Expert
Joined
Jul 5, 2021
Messages
2,712
Solutions
3
Reaction score
2,870
Points
113
Deals
1
Same as in the previous addition with a little excess.
 

Ihml

Don't buy from me
Resident
Language
🇬🇧
Joined
Mar 3, 2024
Messages
25
Reaction score
17
Points
3
Could d-aspartic acid be used instead of d-tartaric acid?
 

Ihml

Don't buy from me
Resident
Language
🇬🇧
Joined
Mar 3, 2024
Messages
25
Reaction score
17
Points
3
Would the lack of solubility of d-aspartic acid in isopropyl alcohol be a problem?
 

handle

Don't buy from me
Resident
Language
🇺🇸
Joined
Apr 16, 2023
Messages
128
Reaction score
77
Points
28
Can D,L Tartaric Acid can be used?
 

handle

Don't buy from me
Resident
Language
🇺🇸
Joined
Apr 16, 2023
Messages
128
Reaction score
77
Points
28
of course not, that would be to easy.. (L)Tartaric acid is extremely expensive here..(D) does not exist here.
Could we use Camphorsulfonic acid instead?
 

Ihml

Don't buy from me
Resident
Language
🇬🇧
Joined
Mar 3, 2024
Messages
25
Reaction score
17
Points
3
L-tartaric acid is like 10 euros per 1 kg where I live. Where are you from?
 

handle

Don't buy from me
Resident
Language
🇺🇸
Joined
Apr 16, 2023
Messages
128
Reaction score
77
Points
28
M3erHqoMFB

Plus some ridiculous freight charge on top.
 

G.Patton

Expert
Joined
Jul 5, 2021
Messages
2,712
Solutions
3
Reaction score
2,870
Points
113
Deals
1
Order that from China here, it would be much cheaper.
 

handle

Don't buy from me
Resident
Language
🇺🇸
Joined
Apr 16, 2023
Messages
128
Reaction score
77
Points
28
Would Camphorsulfonic acid work?
Otherwise I will buy Tartaric Acid from China.
 

G.Patton

Expert
Joined
Jul 5, 2021
Messages
2,712
Solutions
3
Reaction score
2,870
Points
113
Deals
1
I don't know for sure. Probably. There are questions about its solubility and amphetamine adduct solubility with this acid.
 

handle

Don't buy from me
Resident
Language
🇺🇸
Joined
Apr 16, 2023
Messages
128
Reaction score
77
Points
28
When doing the initial salting of the freebase, no precipitation forms? The freebase is now slightly acidic with no product. Can I save it from here? Or is it now rubbish?
 

G.Patton

Expert
Joined
Jul 5, 2021
Messages
2,712
Solutions
3
Reaction score
2,870
Points
113
Deals
1
Hi, can you be more precise with your question please.
 

FENTAMAS

Don't buy from me
Resident
Joined
Feb 2, 2024
Messages
83
Reaction score
68
Points
18
@handle, International team of telepathic chem experts already working with your problem.
Wait for a Skype call when the solution is ready.

But some info is already accessible from universe, we guess the reason is WATER.
 

handle

Don't buy from me
Resident
Language
🇺🇸
Joined
Apr 16, 2023
Messages
128
Reaction score
77
Points
28
Eye eye captain., I'll try it again, this time on a boat? Water, water everywhere but not a drop to drink.
 

dummy dummietis

Don't buy from me
Resident
Language
🇺🇸
Joined
Apr 11, 2024
Messages
12
Reaction score
3
Points
3
What solvents in what proportions shall be used to extract d-amph from racemic?
Of course, I can separate isomers in acetone, but it requires a lot of acetone, around 15+ml per 1g of racemic base. I'm looking for more fast route. Better if salt and unreacted base will stay in different phases after partial acidation.
 
Top