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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084824Generated: October 27, 2026

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

https://huagongshe.com/reaction/2084824

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 numberUS06716987B1
Source datasetuspto-grants-2004_04
ORD IDord-9f3a6b593b9744d5b7b38f219e837247
Source noteuspto-grants-2004_04