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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879875Generated: October 31, 2026

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

https://huagongshe.com/reaction/1879875

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 (0.2 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/EtOAc 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 numberUS08318733B2
Source datasetuspto-grants-2012_11
ORD IDord-4f6c8da5348d4a7e9471896e3775344c
Source noteuspto-grants-2012_11