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1-(3,5-dichloro-4-(propylthio)phenyl)-2-aminopropane.png


JULIE
1-(3,5-dichloro-4-(propylthio)phenyl)-2-aminopropane
 
1-(3,4-di(trifluoromethyl)phenyl)-2-methylaminopropane.png


KATMANDU
1-(3,4-di(trifluoromethyl)phenyl)-2-methylaminopropane

1-(3,4,5-tri(trifluoromethyl)phenyl)-2-aminopropane.png


TIMBUKTU
1-(3,4,5-tri(trifluoromethyl)phenyl)-2-aminopropane
 
1-(3,4-dichlorophenyl)-1-carbomethoxy-2-methylaminopropane.png


GABRIEL
1-(3,4-dichlorophenyl)-1-carbomethoxy-2-methylaminopropa

&

1-(3,4,5-trichlorophenyl)-1-carbomethoxy-2-aminopropane.png


DRESDEN
1-(3,4,5-trichlorophenyl)-1-carbomethoxy-2-aminopropane
 
N-(2,2,2-trifluoroethyl)-1-(3,4-dibromophenyl)-1-carbomethoxy-2-aminopropane.png


ETSY_BETSY
N-(2,2,2-trifluoroethyl)-1-(3,4-dibromophenyl)-1-carbomethoxy-2-aminopropane
 
I Think This Would Work.

1-phenyl-2-propanone.png


Plus Br2,

1-bromo-1-phenyl-2-propanone.png


No se requiere ephedrina.

HO-CH2CH2-OH, ethylene glycol
OH-
Protecting group

1-methyl-1-(1-bromo-1-phenylmethyl)-2,5-dioxacyclopentane.png


KCN, OH-

1-cyano-1-phenyl-2-(1-2,5-dioxacyclopentanyl)propane.png


H3O+

1-carboxy-1-phenyl-2-oxopropane.png


1-phenyl-1-carboxy-2-methylaminopropane.png


HCl, CH3OH

1-phenyl-1-carbmethoxy-2-methylaminopropane.png
 
Last edited:
Rectify said:
I Think This Would Work.

1-phenyl-2-propanone.png


Plus Br2,

1-bromo-1-phenyl-2-propanone.png


No se requiere ephedrina.
Click to expand...

Why not simply obtain L-PAC which is uncontrolled? - you can halogenate that quite simply.

I think a great challenge would be to find a way to produce 4-MA$ from L-PAC in a facile manner. I've spent ages searching with no luck, but it's likely MY limitation rather than a limitation of the chemistry.
 
Last edited:
This Is Simpler Starting With Ephedrine:

1-phenyl-1-hydroxy-2-methylaminopropane.png


Step 1: PBr3

1-phenyl-1-bromo-2-methylaminopropane.png


Step 2: KCN, OH-

1-phenyl-1-cyano-2-methylaminopropane.png


Step 3: Cl-TMS (chloro trimethyl silane)


1-phenyl-1-carbomethoxy-2-methylaminopropane.png


BOUNCE in ONLY 3 STEPS!
 
Last edited:
1-(3,4-methylenedioxyphenyl)-1-oxo-2-methylaminopropane.png


Methylone; 4-mmc

NaBH4

1-(3,4-methylenedioxyphenyl)-1-hydroxy-2-methylaminopropane.png


MD-ephedrine

Cl-(C=O)-Cl

1-(3,4-methylenedioxyphenyl)-1-chloro-2-methylaminopropane.png


KCN, OH-

1-(3,4-methylenedioxyphenyl)-1-cyano-2-methylaminopropane.png


Cl-TMS, chloro trimethyl silane

1-(3,4-methylenedioxyphenyl)-1-carbomethoxy-2-methylaminopropane.png


SUPERSTAR

Only 4 Steps From Methylone!!!!
 
Last edited:
Rectify said:
This Is Simpler Starting With Ephedrine:

1-phenyl-1-hydroxy-2-methylaminopropane.png


Step 1: PBr3

1-phenyl-1-bromo-2-methylaminopropane.png


Step 2: KCN, OH-

1-phenyl-1-cyano-2-methylaminopropane.png


Step 3: Cl-TMS (chloro trimethyl silane)


1-phenyl-1-carbomethoxy-2-methylaminopropane.png


BOUNCE in ONLY 3 STEPS!
Click to expand...
If I were you I would be tempted to contact a university and apply for it on your research thesis. Either that or the fluoxetine analogs made from ephedrine. You said Bounce has been made already though and you have tried it? Another leaving group that could be considered are tosylate or triflate groups.
 
Yes, I tried some Bounce. Part stimulant, part opioid, part dissociative. Mainly stimulant. More potent than methamphetamine in terms of effects and requires a lower dosage. Is a "Dance Drug," like MDMA used to be when I could still get it. I can only, at this point, imagine what Superstar would feel like and whether the MDO-phenyl group can withstand Cl-TMS. You wouldn't happen to know, would you?
 
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