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Benzenehexol

Chemical compound From Wikipedia, the free encyclopedia

Benzenehexol
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Benzenehexol, also called hexahydroxybenzene, is an organic compound with formula C
6
H
6
O
6
or C
6
(OH)
6
. It is a six-fold phenol of benzene.[2][3] The product is also called hexaphenol,[4] but this name has been used also for other substances.[5]

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Benzenehexol is a crystalline solid soluble in hot water,[4] with a melting point above 310°.[2] It can be prepared from inositol (cyclohexanehexol).[citation needed] Oxidation of benzenehexol yields tetrahydroxy-p-benzoquinone (THBQ), rhodizonic acid, and dodecahydroxycyclohexane.[6] Conversely, benzenehexol can be obtained by reduction of sodium THBQ salt with SnCl2/HCl.[7]

Benzenehexol is a starting material for a class of discotic liquid crystals.[7]

Benzenehexol forms an adduct with 2,2'-bipyridine, with 1:2 molecular ratio.[8]

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Benzenehexolate

Like most phenols, benzenehexol can lose the six H+ ions from the hydroxyl groups, yielding the hexaanion C
6
O6−
6
. The potassium salt of this anion is one of the components of Liebig's so-called "potassium carbonyl", the product of the reaction of carbon monoxide with potassium. The hexaanion is produced by trimerization of the acetylenediolate anion C
2
O2−
2
when heating potassium acetylenediolate K
2
C
2
O
2
.[9] The nature of K
6
C
6
O
6
was clarified[10] by Rudolf Nietzki and Theodor Benckiser [de] in 1885, who found that its hydrolysis yielded benzenehexol.[11][12]

The lithium salt of this anion, Li6C6O6 has been considered for electric battery applications.[13]

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Esters

Hexahydroxy benzene forms esters such as the hexaacetate C
6
(-O(CO)CH3)6 (melting point 220 °C) and ethers like hexa-tert-butoxybenzene C
6
(-OC(CH3)3)6 (melting point 223 °C).[9]

References

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