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Author: Subject: Aurin
morsagh
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[*] posted on 24-1-2017 at 09:05
Aurin


Didn´t find anywhere exact procedure for synthesis of aurin from phenol and oxalic acid, can somebody help? Is evolution of carbon monooxide from oxalic acid problem?
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Boffis
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[*] posted on 24-1-2017 at 12:58


The usual condensing agent is anhydrous zinc chloride, See Richter vol 2 p593. He refers to the use of phenol, formic acid and zinc chloride for the preparation of aurin but oxalic acid will probably work too with the evolution of carbon dioxide. If you want an actual reference try looking in one of the older chemical disctionarys such as Thorpes.
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PHILOU Zrealone
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[*] posted on 24-1-2017 at 15:06


Aurin wikipedia

Aurin-synthesis.jpg - 32kB

also good to check other languages like German or Dutch.

Into the german one they give reference 6:
S. Hauptmann, J. Gräfe, H. Remane:
Lehrbuch der organischen Chemie, VEB Deutscher Verlag für Grundstoffindustrie, Leipzig 1980, S. 694.


[Edited on 24-1-2017 by PHILOU Zrealone]




PH Z (PHILOU Zrealone)

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[*] posted on 26-1-2017 at 15:17


I was curious about OP's relatively simple synthesis of aurin. I found the following synthesis in the Journal of the Chemical Society, Transactions.

Redistilled phenol (1,000 grams) was heated with 500 grams of concentrated sulphuric acid and 650 grams of dehydrated oxalic acid in an open flask at 135-145'. Gas evolution ceased after twenty-four hours, and the hot, dark red, viscous mass was poured into a large quantity of cold water.

The pasty deposit was repeatedly digested with several litres of hot water, the dye gradually becoming more viscous in the hot and more brittle in the cold through the elimination of unchanged phenol and soluble by-products. The strongly coloured wash waters were poured into hot, and the red solid deposited by the several wash waters cooling gradually diminished to a negligible amount. The solid deposited by the first wash water amounted to 100 grams. The final wash water was pale yellow and was free from sulphuric acid. The washed dye was freed from water as much as possible by squeezing it while soft and warm. On cooling, it formed a fairly hard mass with a green lustre. Weight, 320-550 grams.

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