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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103046Generated: October 30, 2026

Water → 2,6-Diethylbenzene-1,4-diol

https://huagongshe.com/reaction/2103046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
Reactant2,6-DiethylanilineHCID 11369—
ReactantSodium DithioniteHCID 24489—
ReactantPotassium DichromateHCID 24502—
SolventEthyl AcetateHCID 8857—
Product2,6-Diethylbenzene-1,4-diolHCID 14258205—

Reaction Steps

To a solution of potassium dichromate (20 g) in water (278 mL) was added a solution (60° C.) of 2,6-diethylaniline (15.5 mL) and conc. sulfuric acid (27.8 mL) in water (580 mL). The solution was stirred for 1 hour and then extracted with ethyl acetate. After removing the solvent, the residue was dissolved in acetone (150 mL) and refluxed with water (150 mL) and conc. sulfuric acid (5 mL) for 3 hours. The acetone was removed and the mixture was extracted with ethyl acetate. Evaporation and a quick flash column (silica gel, ethyl acetate-hexane 0% to 5%) gave a residue that was dissolved in ethyl acetate and shaken with an excess of aqueous sodium hydrosulfite. Evaporation gave 3 g of 2,6-diethylbenzene-1,4-diol that was combined with acetyl chloride (13 mL, 14.18 g) in toluene (100 mL) and refluxed for 3 hours. The solvent and the excess reagent were removed under vacuum. The residue was heated up to 110° C. with boron trifluoride-acetic acid complex (14 mL) for 48 hours. Work up and chromatography (silica gel, hexane-ethyl acetate 2% to 10%) gave 4 g of 3-acetyl-2,6-diethyl-4-hydroxyphenyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576094B2
Source datasetuspto-grants-2009_08
ORD IDord-5a833a93334c4e788722360d45bc8a43
Source noteuspto-grants-2009_08