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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380781Generated: November 1, 2026

Hydroquinone → 4-Methoxyphenol

https://huagongshe.com/reaction/380781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroquinoneHCID 785—
ReactantMethylhydroquinoneHCID 7253—
ReactantTrimethylhydroquinoneHCID 12785—
Reactant2,3-DimethylhydroquinoneHCID 69100—
ReactantLithium hydroxide, monohydrateHCID 168937—
SolventMethanolHCID 887—
Product4-MethoxyphenolHCID 9015—
ProductDurohydroquinoneHCID 136346—

Reaction Steps

Into an autoclave (inner volume: 4.5 ml, made of SUS 316, without manometer) were charged 0.031 g of hydroquinone, 1.370 g of methanol and 0.063 mg of lithium hydroxide monohydrate (manufactured by Wako Pure Chemical Ind., Ltd.). The reaction was started by elevating the temperature up to 420° C. with sand bath. After 7 minutes, 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 hydroquinone was 72% by mole, the selectivity of monomethylhydroquinone was 34% by mole, the selectivity of dimethylhydroquinone was 42% by mole and the selectivity of trimethylhydroquinone was 18% by mole. As byproducts, tetramethylhydroquinone and p-methoxyphenol were produced with selectivities of 2% by mole and 1% by mole, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06303801B1
Source datasetuspto-grants-2001_10
ORD IDord-1f60ddf478334f48af70da27ac33a8d0
Source noteuspto-grants-2001_10