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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1847299Generated: October 30, 2026

p-Toluenesulfonic acid → 2-(2,2-Dimethylbenzo[d][1,3]dioxol-5-yl)acetonitrile

https://huagongshe.com/reaction/1847299

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2,2-DimethoxypropaneHCID 6495—
Reactant2-(3,4-Dihydroxyphenyl)acetonitrileHCID 10909727—
SolventTolueneHCID 1140—
Product2-(2,2-Dimethylbenzo[d][1,3]dioxol-5-yl)acetonitrileHCID 5526773220%

Reaction Steps

To a solution of (3,4-dihydroxy-phenyl)-acetonitrile (0.20 g, 1.3 mmol) in toluene (4 mL) was added 2,2-dimethoxy-propane (0.28 g, 2.6 mmol) and TsOH (0.010 g, 0.065 mmol). The mixture was heated at reflux overnight. The reaction mixture was evaporated to remove the solvent and the residue was dissolved in ethyl acetate. The organic layer was washed with NaHCO3 solution, H2O, brine, and dried over Na2SO4. The solvent was evaporated under reduced pressure to give a residue, which was purified by column chromatography on silica gel (petroleum ether/ethyl acetate 10:1) to give 2-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)acetonitrile (40 mg, 20%). 1H NMR (CDCl3, 400 MHz) δ 6.68-6.71 (m, 3H), 3.64 (s, 2H), 1.67 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952050B2
Source datasetuspto-grants-2015_02
ORD IDord-28ff9ebb0f96485c9b25bd6818cbb825
Source noteuspto-grants-2015_02