Sciencemadness Discussion Board
Not logged in [Login ]
Go To Bottom

Printable Version  
Author: Subject: Anthranillic acid from salicyclic acid
WangleSpong5000
Hazard to Others
***




Posts: 129
Registered: 3-11-2017
Location: Oz
Member Is Offline

Mood: Curious

[*] posted on 20-4-2018 at 17:33
Anthranillic acid from salicyclic acid


So the action of nitrous acid/diazonium ion(s) on the lone OH group on the 2 position on the benzene ring can be made into an amino group just as the inverse can be done, but what protects the carbonyl group OH? Is it something to do with the nitrous acid not reacting with this OH group as the double bond on the Oxygen is a kind of resonating structure as part of the carbonyl group and as a result of this the diazonium ion can't be made via the nitrous acid?

Maybe not a resonance structure but the polar equivalent I can't remember the name of?




Hyperbole be thy name
View user's profile View All Posts By User
Chemi Pharma
Hazard to Others
***




Posts: 349
Registered: 5-5-2016
Location: Latin America
Member Is Offline

Mood: Quarantined

[*] posted on 20-4-2018 at 22:22


If you want to convert salicylic acid into anthranilic acid directly, in one pot, follow the direction given by the paper below about conversions of phenols into amines with chloroacetamide, K2CO3, KI, DMF system:

Attachment: phenols to anilines with chloroacetamide, K2CO3, KI and DMF.PDF (1.9MB)
This file has been downloaded 548 times

View user's profile View All Posts By User
byko3y
National Hazard
****




Posts: 721
Registered: 16-3-2015
Member Is Offline

Mood: dooM

[*] posted on 21-4-2018 at 18:35


WangleSpong5000, I don't understand what you mean by "action of nitrous acid/diazonium ion(s) on the lone OH group on the 2 position on the benzene ring can be made into an amino group". Second position relative to what? To NH2 group? Then the ring already contains amino group - why do you need to introduce it?
Benzenediazonium carboxylates are existing compounds, probably unstable though. Carboxylic group requires a lot of energy to be broken.
View user's profile View All Posts By User
LearnedAmateur
National Hazard
****




Posts: 513
Registered: 30-3-2017
Location: Somewhere in the UK
Member Is Offline

Mood: Free Radical

[*] posted on 22-4-2018 at 02:00


Nitrous acid reacts with OH groups to form nitrite esters, which are good protecting groups, but don’t form amines. Nitrous acid reacts with amines to form diazonium salts, which are not useful at all in this case since the nitrogen will leave the reaction as N2, the Sandmeyer reaction. So, it’s easy to make salicylic acid from anthranilic acid via that method (reaction with H2O to replace -NH2 with -OH) but I don’t think nitrous acid would be overly useful for the other way around.

[Edited on 22-4-2018 by LearnedAmateur]




In chemistry, sometimes the solution is the problem.

It’s been a while, but I’m not dead! Updated 7/1/2020. Shout out to Aga, we got along well.
View user's profile View All Posts By User
Texium
Administrator
Thread Moved
22-4-2018 at 15:46

  Go To Top