Author Topic: What about riping of the -OH of chavicol?  (Read 1863 times)

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malvaxman

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What about riping of the -OH of chavicol?
« on: September 08, 2001, 05:08:00 PM »
What about riping of the OH- of chavicol ?

OH-Ph-CH2-CH=CH2

,or replace it with a F.

How is it done in the best way, does anyone have any sugestions?
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https://www.thevespiary.org/rhodium/Rhodium/chemistry/yadontsay/index.html


Rhodium

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Re: What about riping of the -OH of chavicol?
« Reply #1 on: September 09, 2001, 04:29:00 AM »
You cannot easily get rid of oxygens stuck to aromatic rings. The only thing you can do is to alkylate it to an ether with an alkyl halide/K2CO3/acetone for example.