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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057941Generated: October 26, 2026

p-Toluenesulfonic acid → 4-Methoxy-2,2-dimethyl-1,3-benzodioxole

https://huagongshe.com/reaction/1057941

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3-MethoxycatecholHCID 13622—
ReactantSodium HydroxideHCID 14798—
SolventBenzeneHCID 241—
Product4-Methoxy-2,2-dimethyl-1,3-benzodioxoleHCID 15061094—

Reaction Steps

3-Methoxycatechol (25 g) was dissolved in benzene, and dimethoxyacetal (35 ml) and a catalytic amount of p-toluenesulfonic acid were added thereto, followed by heating at reflux for 6 hours. After being allowed to stand for cooling, the mixture was adjusted to alkaline with an aqueous solution of sodium hydroxide, followed by extraction with ether. The organic layer was washed with a saturated saline and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=99/1) to give Compound IIbk-a (19.4 g, 60.5%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06514996B2
Source datasetuspto-grants-2003_02
ORD IDord-b56b9681518f4d3ebb66dfcc047e363d
Source noteuspto-grants-2003_02