Derek McOlund
Harmless
Posts: 11
Registered: 28-11-2016
Member Is Offline
Mood: No Mood
|
|
Benzene ---> Phenol
Have anyone an idea of how to turn benzene to phenol? I know of the cumene process, but is there any easier method? I've heard that you'd extract
phenol from coal tar back in the days, does anyone know how that can be done?
I know that phenol can be reduced to benzene using zinc
C6H5OH + Zn → C6H6 + ZnO, but can you oxidize benzene to obtain phenol?
|
|
|
unionised
International Hazard
Posts: 5103
Registered: 1-11-2003
Location: UK
Member Is Offline
Mood: No Mood
|
|
Chlorination then hydrolysis of chlorobenzene is an alternative, but it's not any easier than the cumene process.
|
|
|
CuReUS
National Hazard
Posts: 928
Registered: 9-9-2014
Member Is Offline
Mood: No Mood
|
|
previously,the direct hydroxylation of arenes was done by fenton's reagent.But the reaction is messy and the yield is poor,so over the years there
have been many modifications.
|
|
|
DDTea
National Hazard
Posts: 940
Registered: 25-2-2003
Location: Freedomland
Member Is Offline
Mood: Degenerate
|
|
Natural and synthetic P450's, such as the Groves metal porphyrin catalysts and improvements thereupon (Dolphin-Chorghade system has best performance
as far as I know), will oxidize benzene to phenol. The trouble is they don't *stop* at phenol, and will oxidize benzene all the way to benzoquinone.
The catalytic oxidation of benzene to phenol using atmospheric oxygen or H2O2 would be of enormous commercial significance. It would be an
improvement in atom economy over the existing cumene process.
Addendum:
Additionally, N2O has been used to oxidize benzene to phenol over zeolite catalysts. Selectivity for phenol is high but conversions are low (20 -
25%). Google turned up a ton of papers with the search terms "benzene" "N2O" "phenol."
The story isn't much different with homogeneous catalysts, it seems. Here's a homogeneous nickel catalyst that hydroxylates benzene with H2O2 to
selectively form phenol, with <1% benzoquinone.
http://pubs.acs.org/doi/abs/10.1021/jacs.5b01814
Outside the realm of catalysis, phenyl lithium and phenyl magnesium bromide may be converted to phenol in good yields. These are stoichiometric
reactions, of course, and would require pre-synthesis of the organometallic reagent from bromobenzene. Thus it becomes a two-step process, and the
oxidants aren't readily available to the amateur (tert-butylhydroperoxide).
This is an interesting research question. If you can find a good way to form a phenyl radical from benzene (a high energy endeavor, for sure) and to
quench it with H2O2, you might have the beginnings of a pathway to phenol.
[Edited on 12-4-16 by DDTea]
"In the end the proud scientist or philosopher who cannot be bothered to make his thought accessible has no choice but to retire to the heights in
which dwell the Great Misunderstood and the Great Ignored, there to rail in Olympic superiority at the folly of mankind." - Reginald Kapp.
|
|
|
Texium
|
Thread Moved
4-12-2016 at 14:17 |
UC235
National Hazard
Posts: 565
Registered: 28-12-2014
Member Is Offline
Mood: No Mood
|
|
If this is a theoretical question, see above. If you've a practical interest in preparing phenol, see my writeup in Prepublication subforum starting
from aspirin/salicylic acid.
|
|
|
S.C. Wack
bibliomaster
Posts: 2419
Registered: 7-5-2004
Location: Cornworld, Central USA
Member Is Offline
Mood: Enhanced
|
|
Nitration or sulfonation first.
|
|
|
![[*]](images/xpblue/default_icon.gif){kind=icon}
