morsagh
Hazard to Others
Posts: 187
Registered: 20-2-2014
Member Is Offline
Mood: No Mood
|
|
Alizarin synthesis
Can be alizarin produced by Friedel-Crafts reaction of phtalic anhydride and catechol? What should be used as catalyst? ZnCl2 or conc. H2SO4 (with
H2SO4 will be easier to work)? Can be alizarin used for production of dihydroxybenzanthrone by reaction with glycerol and copper. Thank you very much
for help.
|
|
|
Nicodem
|
Thread Moved
23-4-2016 at 07:57 |
unionised
International Hazard
Posts: 5103
Registered: 1-11-2003
Location: UK
Member Is Offline
Mood: No Mood
|
|
"Can be alizarin produced by Friedel-Crafts reaction of phtalic anhydride and catechol?"
Maybe, but if you do the reaction in the presence of sulphuric acid you get something else
http://www.forgottenbooks.com/readbook_text/Allens_Commercia...
I suspect that, in the rpesence of the usual FC catalysts you will get something like this
https://chimique.files.wordpress.com/2010/11/synthesis-of-fl...
rather than alizarin
|
|
|
UC235
National Hazard
Posts: 565
Registered: 28-12-2014
Member Is Offline
Mood: No Mood
|
|
Nope. FC-acylation and phenols don't play nice. Even if the phenols were protected as ethers, the 2,3-product would probably dominate the reaction
products.
While alizarin is regarded as the first synthetic version of a natural pigment, my reading on the subject showed that this is a bit of a stretch. The
"alizarin" was produced by bromination of anthraquinone under pressure followed by fusion with alkali hydroxides. This produced a mixture of
polyhydroxyanthraquinones, not merely 1,2-dihydroxyanthraquinone. Functionally it dyed fabric in a similar manner but possibly with different
light-fastness and color shade.
An improved prep starts with anthraquinone, sulfonates it with oleum, and isolates sodium anthraquinone-2-sulfonate (Silver salt). On fusion with
alkali hydroxide and nitrate, alizarin is produced. I can't find my reference paper for this synthesis however.
It can also be made from o-dichlorobenzene and phthalic anhydride. On fusion with alkali, the 2,3-dichloroanthraquinone dehalogenates and rearranges
to alizarin.
I am also attaching a prep of radiolabelled alizarin. While most of the prep is impractical as a reasonable alizarin synthesis, the last step is an
oxidation of 2-hydroxyanthraquinone to alizarin using alkali and chlorate that may prove useful.
Attachment: Alizarin Synthesis_o-DCB.pdf (392kB)
This file has been downloaded 823 times
Attachment: Alizarin- Synthesis of radiolabelled material.pdf (512kB)
This file has been downloaded 447 times
[Edited on 23-4-2016 by UC235]
[Edited on 23-4-2016 by UC235]
|
|
|
Boffis
International Hazard
Posts: 1836
Registered: 1-5-2011
Member Is Offline
Mood: No Mood
|
|
You don't need a FC reaction; Phthalic anhydride and catachol react in conc. sulphuric acid but the main products are tars, hydroxyphenylxanthines and
2,3-dihydroxyanthroquinone, only a little 1,2-dihydroxyanthraquinone is produced. It is described in an old book I have on anthraquinone dyes but I
don't have it with me so I can't give you a reference but the reaction was described under the 2,3 dihydroxy compound as the original method of
preparation of this compound. The seperation is tedious though and the total yield of both compounds poor.
|
|
|
morsagh
Hazard to Others
Posts: 187
Registered: 20-2-2014
Member Is Offline
Mood: No Mood
|
|
Are there any conditions like refluxing Boffis? Sounds interesting, I´ll try it.
|
|
|
CuReUS
National Hazard
Posts: 928
Registered: 9-9-2014
Member Is Offline
Mood: No Mood
|
|
yes
http://www.google.co.in/patents/US20050267307
there is another method from pthaloyl chloride and catecol
"Sartori, Giovanni; Casnati, Giuseppe; Bigi, Franca; Foglio, Federica Gazzetta Chimica Italiana, 1990 , vol. 120, # 1 p. 13 - 19"
|
|
|
morsagh
Hazard to Others
Posts: 187
Registered: 20-2-2014
Member Is Offline
Mood: No Mood
|
|
Product after reacting catechol and phthalanhydride in conc. sulphuric acid. Do you think it is mostly 1,2 dihydroxyantraquinone or 2,3?
|
|
|
Pumukli
National Hazard
Posts: 686
Registered: 2-3-2014
Location: EU
Member Is Offline
Mood: No Mood
|
|
Dunno, I'd prefer it would be the 1,2-dihydroxy variety. :-)
Anyway, if you want less uncertainty but a similar nice dye then you should start from hydrochinone instead of catechol. This way the reaction should
yield purpurin, which is the 1,4-dihydroxy compound.
If you had the 1,2-dihydroxy compound (alizarin) then you could nitrate it and the nitro group should move to position 3. The resulting compound is
alizarin orange and it has (or so they say) a nice orange color. :-)
|
|
|
Boffis
International Hazard
Posts: 1836
Registered: 1-5-2011
Member Is Offline
Mood: No Mood
|
|
@Morsagh
I have found a reference to the sulphuric acid condensation that is exactly what I described above: check out Berichte 1888 v21 p2503. A Schoeller. He
used 5g of catechol and 6.5g of phthalic anhydride in 75g of conc sulphuric acid for 4.5 hours at 140-145 deg C. He goes on to describe the work up.
Also worth a look is:
Berichte v28 p116; K Lazodzinski 1895; FC condensation in carbon disulphide; phthalic anhydride + dimethyl ethers of dihydroxyphenols to the
appropriate dimethoxyanthraquinone (veratrole gives mainly 2,3-methoxyanthraquinone and by hydrolysis of the ether hystazarin or
2,3-dihydroxyanthraquinone). Also covers the condensation of hydroquinone dimethyl ether to give ultimately Quinizarin
Another ref (Berichte v35 p1778) found that prolonged digestion of hystazarin in conc sulphuric acid results in partial convertion to alizarin. This
may explain the alizarin found by Schoeller.
|
|
|
morsagh
Hazard to Others
Posts: 187
Registered: 20-2-2014
Member Is Offline
Mood: No Mood
|
|
I will try next time that with hydroquinone, don´t you know how to extract purpurine and how to extract alizarin/nitroalizarin?
|
|
|
Pumukli
National Hazard
Posts: 686
Registered: 2-3-2014
Location: EU
Member Is Offline
Mood: No Mood
|
|
Corrections to my previous comment in this thread:
1,4-dihydroxy-anthraquinone is NOT purpurin. It is called quinizarin. Purpurin is a derivative of quinizarin, it is 1,2,4-trihydroxy-anthraquinone. (I
mixed up the common names, sorry.)
The industrial quinizarin synthesis starts from p-chloro-phenol instead of hydrochinone. Starting from the later is possible too, but requires working
with molten AlCl3/NaCl mixture and the yield is still very low. :-(
P-chloro-phenol is condensed with phthalic anhydride with H2SO4 and boric acid. Boric acid continuously removes the forming
quinizarin by esterification from the mixture and turns the equilibrium reaction into a one-way route.
You can read about anthraquinone dye chemistry here:
Bien, H.-S.; Stawitz, J.; Wunderlich, K. (2005), "Anthraquinone Dyes and Intermediates", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim:
Wiley-VCH, doi:10.1002/14356007.a02_355
Edit:
Orgsyn has a quinizarin preparation too:
http://www.orgsyn.org/demo.aspx?prep=CV1P0476
And prepchem has the quinizarine synth. starting from hydrochinone and using sulfuric acid, claiming 20% yield:
http://www.prepchem.com/synthesis-of-quinizarin/
[Edited on 27-4-2016 by Pumukli]
|
|
|
![[*]](images/xpblue/default_icon.gif){kind=icon}
