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Phenyl-2-Propanone
Phenyl-2-Propanone (Phenylacetone, P2P) is a ketone. It can be used in reductive amination with either ammonia, methylamine, ethylamine, or propylamine in an ethanol and hydrogen oxide(water) solution. It forms an imine intermediate. The reductive amination can be done with either toxic Aluminum Mercury or nontoxic Aluminum Galinstan. As a result, you can get amphetamine, methamphetamine, Ethylamphetamine, or Propylamphetamine. Using methylamine, ethylamine, or propylamine will yield around 70% methamphetamine, Ethylamphetamine, or Propylamphetamine, while using ammonia will yield 30% amphetamine. Ethylamphetamine is Blue Speed.
Phenyl-2-Propanone can be synthesized from benzyl magnesium chloride (formed from benzyl chloride and magnesium turnings in diethyl ether) and acetonitrile in diethyl ether (or better, dibutyl ether for higher yield) followed by hydrochloric acid work-up.
Phenyl-2-Propanone can be synthesized from benzyl magnesium chloride (formed from benzyl chloride and magnesium turnings in diethyl ether) and acetonitrile in diethyl ether (or better, dibutyl ether for higher yield) followed by hydrochloric acid work-up.
I used Phenyl-2-Propanone (P2P) in reductive amination with an ethanol water solution of ethylamine using Aluminum Galinstan. I got Ethylamphetamine. Blue Speed.
Phenyl-2-Propanone by CognitiveFuel November 30, 2022
Related Words
probano • probono • Probane smith • Proano • probalogical • probalogically • Probang • probankle • probonotobly • probsnotok
no probalo
no probalo by Tyler Sadex June 29, 2004
3,4-MethyleneDioxyPhenyl-2-Propanol
3,4-MethyleneDioxyPhenyl-2-Propanol (MDP2Pol) is a chemical with a boiling point of 125°C at 25mmHg. MDP2Pol is a yellowish oil which is an alcohol. It is formed from dilute phosphoric acid hydration of safrole (sulfuric acid isn't used because sulfuric acid is an oxidizing acid which rearranges MDP2Pol (3,4-MethyleneDioxyPhenyl-2-Propanol) to MDP1Pol (3,4-MethyleneDioxyPhenyl-1-Propanol). MDP2Pol is also formed by oxymercuration demercuration of safrole. MDP2Pol can be oxidized to MDP2P (3,4-MethyleneDioxyPhenyl-2-Propanone) by either sodium chlorite or sodium hypochlorite in hydrochloric acid and the byproduct is chlorine gas (wear a gas mask and do the reaction outside). It can also be oxidized by lead acetate. 3,4-MethyleneDioxyPhenyl-2-Propanol is also called Sesamyl-2-Propanol (Se2Pol, Ses2Pol, Sm2Pol), hydroxysafrole, and Sesamylisopropanol.
I formed 3,4-MethyleneDioxyPhenyl-2-Propanol by hydrating safrole with an aqueous dilute solution of phosphoric acid.
3,4-MethyleneDioxyPhenyl-2-Propanol by CognitiveFuel November 18, 2022
3,4-MethyleneDioxyPhenyl-2-Propanone
3,4-MethyleneDioxyPhenyl-2-Propanone (MDP2P) is a yellow chemical that has a melting point of 87-88 °C and a Boiling point range of 115-170 °C at around 30 mmhg. MDP2P can be synthesized by oxidation of MDP2Pol (3,4-MethyleneDioxyPhenyl-2-Propanol) using either sodium chlorite or sodium hypochlorite in hydrochloric acid and a byproduct is chlorine gas (if hydrochloric acid isn't used, then you will get the haloform reaction). MDP2P can also be synthesized by a grignard reaction of 3,4-MethyleneDioxyBenzyl magnesium chloride (formed from 3,4-Methylenedioxybenzyl chloride and magnesium turnings in diethyl ether) and acetonitrile followed by hydrochloric acid work-up. MDP2P can also be synthesized from wacker oxidation of safrole. Reaction of MDP2P with an ethanol solution of ethylamine and Aluminum Galinstan amalgam reduces the MDP2P-ethylimine intermediate into MDEA. 3,4-MethyleneDioxyPhenyl-2-Propanone is a yellow oily ketone. It is yellow green in the sunlight. MDP2P can also be synthesized by reacting sesamyl tosylate (SmOTs,3,4-Methylenedioxyphenyl tosylate) with ethyl acetoacetate and sodium ethoxide and Copper iodide catalyst and heat. 3,4-MethyleneDioxyPhenyl-2-Propanone is also called Sesamyl-2-Propanone (Se2P, Ses2P, Sm2P), Sesamylacetone, and Piperonyl Methyl Ketone.
I synthesized 3,4-MethyleneDioxyPhenyl-2-Propanone (MDP2P) by reacting 3,4-MethyleneDioxyBenzyl magnesium chloride and acetonitrile followed by hydrochloric acid work-up.
3,4-MethyleneDioxyPhenyl-2-Propanone by CognitiveFuel October 29, 2022
Phenyl-2-Propanol
Phenyl-2-Propanol is a chemical synthesized by reacting benzylmagnesium chloride with acetaldehyde in diethyl ether (or dibutyl ether), or by reacting phenylacetaldehyde (or PAL synthesized from styrene and peracetic acid in a nitrogen or argon atmosphere to avoid over oxidation to phenylacetic acid (PAA) ) with methylmagnesium iodide in diethyl ether (or dibutyl ether). Phenyl-2-Propanol is also known as P2Pol. Phenyl-2-Propanol can be oxidized to Phenyl-2-Propanone by using PCC, or by using Sodium Hypochlorite (pool shock, NaOCl), and glacial acetic acid. P2Pol can also be oxidized to P2P by using Sodium Chlorite (NaO2Cl), and acetic acid.
Density 0.996
Boiling point 220 ºC
Refractive index 1.5221
Flash point 85 ºC
Colorless liquid.
Density 0.996
Boiling point 220 ºC
Refractive index 1.5221
Flash point 85 ºC
Colorless liquid.
Tyler: I synthesized P2Pol (Phenyl-2-Propanol) by reacting phenylacetaldehyde and methylmagnesium iodide in diethyl ether.
Phenyl-2-Propanol by CognitiveFuel August 18, 2023
Propanolol
Conversation 1:
Student 1: "Hey, did you prepare today's seminar?"
Student 2: "Propanolol"
Conversation 2:
Student 3: "HAHAAHAH you said monosynaptic instead of monosyllabic propanolol"
Student 1: "Hey, did you prepare today's seminar?"
Student 2: "Propanolol"
Conversation 2:
Student 3: "HAHAAHAH you said monosynaptic instead of monosyllabic propanolol"
Propanolol by Esparrec January 23, 2017
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