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Dresden's Chemical Fluff Thread (Name-A-Molecule)

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


Cl-(C=O)-Cl

1-phenyl-1-chloro-2-methylaminopropane.png


sodium phenoxide

1-phenyl-1-phenoxy-2-methylaminopropane.png


NOM DE PLUME LE_PENN
1-phenyl-1-phenoxy-2-methylaminopropane
 
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sodium%203,4-methylenedioxyphenoxide.png


sodium 3,4-methylenedioxyphenoxide
from sesamol

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


1-phenyl-1-chloro-2-methylaminopropane.png


1-phenyl-1-(3,4-methylenedioxyphenoxy)-2-methylaminopropane.png


ASHLEY
1-phenyl-1-(3,4-methylenedioxyphenoxy)-2-methylaminopropane
 
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1-(3,4-methylenedioxyphenyl)-1-oxo-2-methylaminopropane.png


METHYLONE
1-(3,4-methylenedioxyphenyl)-1-oxo-2-methylaminopropane

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


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


NaOMe (sodium methoxide)

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


BATMAN
1-(3,4-methylenedioxyphenyl)-1-methoxy-2-methylaminopropane
 
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O-acetyl-1-phenyl-2-methylamino-1-hydroxypropane.png


G7
O-acetyl-1-phenyl-2-methylamino-1-hydroxypropane

^--ephedrine + acetic andydride

2,4-dioxo-3-oxapentane.png


2,4-dioxo-3-oxapentane

But still. The N needs protecting somehow for that to happen.
 
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From methylone

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


WAKE_UP
1-(3,4-methylenedioxyphenyl)-1-phenoxy-2-methylaminopropane

Likewise, starting with methylone using sodium 3,4-MDO-PhenOxide instead of sodium phenoxide:

1-(3,4-methylenedioxyphenoxy)-2-methylamino-1-(3,4-methylenedioxyphenyl)-propane.png


MY_SUPER_SWEET_16
1-(3,4-methylenedioxyphenoxy)-2-methylamino-1-(3,4-methylenedioxyphenyl)-propane

1,1-bis-(3,4-methylenedioxyphenyl)-2-aminopropane.png


BIS_TRIS_TETRAKIS
1,1-bis-(3,4-methylenedioxyphenyl)-2-aminopropane
 
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Ladies & Gentlemen,
It's Time. I Would Like To Present Something...Stronger.

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


BATMAN
1-(3,4-methylenedioxyphenyl)-1-methoxy-2-methylaminopropane
 
1-(2,4,6-trimethoxy-3,5-dibromophenyl)-2-aminopropane.png


CHRISTOPHER
1-(2,4,6-trimethoxy-3,5-dibromophenyl)-2-aminopropane; tma-6 / Br2 / FeBr3

Bromo phenyls are ring deactivating, while methoxies are activating. Should feel kind of like a speedball (a strong upper mixed with a strong downer).
 
sodium%204-allyl-2-methoxyphenoxide.png


CH3CH2-Br

--> Wacker --> ammonium formate Leuckart, etc.

1-(3-methoxy-4-ethoxyphenyl)-2-aminopropane.png


C_LOVE
1-(3-methoxy-4-ethoxyphenyl)-2-aminopropane
 
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1-phenyl-1-carbomethoxy-2-methylaminopropane.png


REX
1-phenyl-1-carbomethoxy-2-methylaminopropane

My best idea yet. Pricey, but worth it.
 
1-aza-2-methyl-3-phenyl-4-oxa-5-oxo-cyclohexane.png


OXO-PRELUDIN
1-aza-2-methyl-3-phenyl-4-oxa-5-oxo-cyclohexane

I really have no clue how to synthesize this lactone, to be perfectly honest. Okay, here goes my best guess.

1-phenyl-1-hydroxy-2-aminopropane.png


PPA
1-phenyl-1-hydroxy-2-aminopropane

1,2-dichloro-1-oxoethane.png


1,2-dichloro-1-oxoethane

I dunno. Something like that.
 
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Similarly,

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


1-(3,4-methylenedioxyphenyl)-1-hydroxy-2-aminopropane (from MDC)

Cl-CH2(C=O)-Cl

1-aza-2-methyl-3-(3,4-methylenedioxyphenyl)-4-oxa-5-oxo-cyclohexane.png


SANTA_MONICA_HIGH_ROLLER
1-aza-2-methyl-3-(3,4-methylenedioxyphenyl)-4-oxa-5-oxo-cyclohexane
 
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1-(3,4-methylenedioxyphenyl)-2-aminopropane.png


THIN_MINTS
1-(3,4-methylenedioxyphenyl)-2-aminopropane

Raver Amy's Favorite!
 
1-allyl-3,4-methylenedioxybenzene.png


1-allyl-3,4-methylenedioxybenzene

1-(propenyl)-3,4-methylenedioxybenzene.png


1-(propenyl)-3,4-methylenedioxybenzene

1-(3,4-methylenedioxyphenyl)-methanone.png


1-(3,4-methylenedioxyphenyl)-methanone

1-methyl-3,4-methylenedioxybenzene.png


MI_PARFUM
1-methyl-3,4-methylenedioxybenzene
 
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