Author Topic: phenylalanine --> PAA  (Read 2517 times)

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ChemicalSolution

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phenylalanine --> PAA
« on: April 25, 2002, 02:37:00 AM »
Finally a use for this stuff?? 

phenylalanine ---> alpha-bromo-phenyl propionic acid via Sandmeyer reaction using KBr, HBr, NaNO2 @0C (dont' know if this will work on phenylalanine)

The bromo acid derivative is converted into 2-phenyl nitro ethane via US pat 4319059..  The procedure involves stirring in DMSO with Mg2+ ion.  This patent uses smaller bromo acids..   Again, not sure if this will work on THIS bromo acid..

2-phenyl nitro ethane is converted into PAA in very high yields using 1mmole nitroalkane, 3mmole NaNO2, 10mmole GAA in DMSO..

She THINKS this one is from JOC 62 234 1997 but she isn't 100% sure so don't throw a fit if she's wrong..

xoxo
Julia

Elementary

  • Guest
Straight oxidisation
« Reply #1 on: April 26, 2002, 01:00:00 AM »
Wouldn't a straight oxidisation of phenylalanine to PAA (phenylacetic acid) be easier ?

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Aurelius

  • Guest
Oxidation
« Reply #2 on: April 26, 2002, 06:42:00 AM »
How do you suggest doing that?

Antoncho

  • Guest
A simpler suggestion...
« Reply #3 on: April 26, 2002, 08:20:00 AM »
Hey, Julie! ;)  (you wouldn't mind me calling you Julie, would you, please?)

... don't know for sure if it'll work, but no reason why it should.

Oxidize phenylalanine into phenylacetaldehyde w/hypoclrorite a la the proc. for tryptophane on Rh's page...

Then oxidize it to PAA or directly make P2P w/CH3I Grignar :)


Antoncho

Elementary

  • Guest
Some search engine results !
« Reply #4 on: April 26, 2002, 02:47:00 PM »
Threads starting with :

Post 258083 (missing)

(Elementary: "Phenylethyl Alcohol Via  L-phenylalanine", Stimulants)

Post 248773 (missing)

(timsong: "Oxidation Of Phenylalanine", Stimulants)


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Elementary

  • Guest
More Info
« Reply #5 on: May 22, 2002, 10:05:00 PM »
I been doing some digging around on the conversion of (L)phenylalanine to phenylacetaldehyde and come up with these bits of information :

http://beers.cz/kvas/1999/3_99/savela.htm



Pyrolytic conversion of phenyalanine to phenylacetaldehyde

http://www.cis.tugraz.at/ilct/MainDis.htm



Ignite a small amount of L-phenylalanine in a gas: the characteristic odor of phenylacetaldehyde is perceptible.

To 5ml of a solution of L-phenylalanine(0.2-100) add 3 drops of potassium bichromate solution and heat: the characteristic odor of phenylacetaldehyde is perceptible.

http://my.ecplaza.net/miwontrading/1.asp



And an article on the Strecker-reaction

http://dfa.leb.chemie.tu-muenchen.de/EJahr2001.html




Don't cry for me I'm the cleaner

Lem2

  • Guest
hey antoncho, if you react phenylacetaldehyde w/ ...
« Reply #6 on: May 23, 2002, 11:09:00 PM »
hey antoncho, if you react phenylacetaldehyde w/ MeAmine first to form the imine, then hit it w/ MeMgI, you get methamphetamine w/o going through p2p. :P

He who makes a beast of himself gets rid of the pain of being a man.