indol conversion | HELP |

lamer

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Structure-of-indole.png
--- indole

7ba42fbb-c8f0-4938-b13d-3290ed5ace21.png
Indol-3-Bütirik Asit

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First of all, hello, I'm Lamer from the forum.

There is no direct indole in my country and it is on the list of controlled chemicals.

Indole-3-butyric acid (IBA) is on sale in my country.

How can I convert Indole-3-Butyric Acid into plain indole, their molecular structures are identical?

I just want to know how to parse it, I would be glad if you can help me.

Every theoretical knowledge is important to me, thank you for my research.


@WillD
@G.Patton

see​
 

Osmosis Vanderwaal

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Consider 3-butryl-glyceraldahyde?
Thats based on the synthesis diagram here

 

lamer

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I'm sorry we can't predict this in my country
 
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WillD

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In what status is it prohibited? Your version of conversion does not seem possible to me, at least in the first study. You can also choose indole-3-carboxylic acid (but not for 018).
 

Osmosis Vanderwaal

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Solely based on this scheme . May theory was simply if it takes 3-phospho-glyceraldehyde to reduce indole-3glycerol phosphate, then it would take 3-butry glyceraldehyde to reduce indole 3 butric acidl
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WillD

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Relevant biosynthesis inside the organism, but I do not think that it will be cost effectively synthetically. But in any case, it is interesting.
 

HIGGS BOSSON

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This is the first time I hear that indole has been banned somewhere. Indole cannot be obtained in the way you proposed, maybe it will be easier for you to replace indole with a legal analogue in your country, for example, methyl-indole?
 

lamer

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There must be an indole suitable for jwh 018 synthesis.
 

HIGGS BOSSON

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For synthesis JWH you can replace indole to 2-methyl-indole. You will obtain JWH-007
JWH-007 displayed optimum binding of 9.50 nM at CB1 and 2.94 nM at CB2


 

lamer

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but this is available
https://www.labmarketi.com/urun/methyl-indole-2-carboxylate-1

not available in our country im from turkey
 
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