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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925785Generated: October 29, 2026

Catechol → 2,3,6,7,10,11-Hexahydroxytriphenylene

https://huagongshe.com/reaction/1925785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCatecholHCID 289—
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
CatalystBis(iron(2+));tris(oxygen(2-))HCID 131728961—
SolventAcetonitrileHCID 6342—
Product2,3,6,7,10,11-HexahydroxytriphenyleneHCID 1108861045.5%

Reaction Conditions

Temperature30 °C

Reaction Steps

Catechol (22.0 g, 0.2 moles) and diiron trioxide (ferric oxide) (31.9 g, 0.2 moles) were added into water (110 mL), and 98% sulfuric acid (440 g, 4.4 moles) was added dropwise to the solution while temperature of the solution was maintained at 30° C. or lower, to adjust the concentration in percent by weight of sulfuric acid in the reaction system at 80%. The solution was reacted at 30° C. for 6 hours with stirring. After completion of the reaction, water (500 mL) was added dropwise to the reaction solution, and the reaction solution was stirred for another 30 minutes. The resultant precipitate was collected by filtration, and the obtained crude crystal was washed with water and dried to give crude crystal (19.2 g). After a part of the crude crystal (5.0 g among 19.2 g) was dispersed in a mixed solvent of water (50 mL) and acetonitrile (200 mL), the dispersion liquid was heated up and stirred for 1 hour. After that, this dispersion liquid was filtered in hot state to filter off insoluble matter, the filtrate was then concentrated under reduced pressure, and the precipitated crystal was collected by filtration, and then dried, to give 2,3,6,7,10,11-hexahydroxytriphenylene (2.56 g, theoretical yield from catechol: 45.5%) in black powder form. 1H-NMR data of the obtained 2,3,6,7,10,11-hexahydroxytriphenylene measured were in accordance with those of 2,3,6,7,10,11-hexahydroxytriphenylene described in the reference. Also, the measurement results of 1H-NMR are shown below. In addition, content of iron ion in the obtained crystal was measured by inductively-coupled plasma optical emission spectroscopy (ICP-OES), and was found that content of iron ion (reduced quantity from metal iron) in the obtained 2,3,6,7,10,11-hexahydroxytriphenylene (2.56 g) was 0.087 mg (0.034 mg/g). Also, the measurement of iron ion content by inductively-coupled plasma optical emission spectroscopy was carried out using inductively-coupled plasma optical emission spectrometer SPS 3100 (manufactured by SII Nanotechnology Inc.) as follows. Several samples containing appropriate amount of metal iron dissolved in n-methyl-2-pyrrolidone were measured and a calibration curve was obtained based on the measurement results, in advance. Content of iron ion in 2,3,6,7,10,11-hexahydroxytriphenylene was obtained from the calibration curve.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178731B2
Source datasetuspto-grants-2012_05
ORD IDord-7a1dddc7984e4626aee627cf4c4f2aaa
Source noteuspto-grants-2012_05