Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380774Generated: October 26, 2026

Methylhydroquinone → Durohydroquinone

https://huagongshe.com/reaction/380774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylhydroquinoneHCID 7253—
ReactantTrimethylhydroquinoneHCID 12785—
Reactant2,3-DimethylhydroquinoneHCID 69100—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductDurohydroquinoneHCID 136346—

Reaction Steps

Into an autoclave (inner volume: 9 ml, made of SUS 316, equipped with a manometer) were charged 0.108 g of methylhydroquinone, 3.573 g of methanol and 0.2 mg of sodium methylate. The reaction was started by elevating the temperature up to 350° C. with sand bath. The pressure during the reaction was 16 MPa. After 4 hours, the autoclave was quickly cooled and the reaction solution was taken out from the autoclave when the temperature was cooled back to the room temperature. The measurement according to the process described above revealed that the conversion of methylhydroquinone was 86% by mole, the selectivity of dimethylhydroquinone was 38% by mole, the selectivity of trimethylhydroquinone was 37% by mole and no tetramethylhydroquinone was produced. As byproducts, methyl ethers of monomethylhydroquinone, dimethylhydroquinone and trimethylhydroquinone, represented by the formulae shown above, were formed with a selectivity of 6%, 4% and 3%, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06303801B1
Source datasetuspto-grants-2001_10
ORD IDord-2f89a487dff242c6bbc0ea7b9ebf3e32
Source noteuspto-grants-2001_10