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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385564Generated: October 31, 2026

Water → 4-Cyanobenzaldehyde

https://huagongshe.com/reaction/1385564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium PersulfateHCID 62655—
Reactant4-(Aminomethyl)benzonitrileHCID 82608—
SolventMethanolHCID 887—
Product4-CyanobenzaldehydeHCID 6604258.8%

Reaction Steps

13.2 g of p-cyanobenzylamine, 28.6 g of sodium persulfate, 10 ml of water, and 100 ml of methanol were mixed and allowed to react at 50° C. for 40 minutes while stirring. After cooling the reaction mixture to room temperature, methanol was distilled off to precipitate solids. To the resulting suspension was added dichloromethane for extraction. The organic layer was washed twice with saturated aqueous sodium bicarbonate solution and then twice with water, and then magnesium sulfate was added thereto. The residue after distilling off dichloromethane was subjected to silica gel column chromatography (eluant: hexane/ethyl acetate=5/1), and hexane and ethyl acetate were distilled off. The resultant crude product concentrated to dryness was recrystallized from cyclohexane, the crystals were filtered, and dried to obtain 7.7 g (yield: 58%) of p-cyanobenzaldehyde. The obtained p-cyanobenzaldehyde had a purity of 99% by the analysis of high performance liquid chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262292B1
Source datasetuspto-grants-2001_07
ORD IDord-7e646b1f8a564728b3686e9a0377ad56
Source noteuspto-grants-2001_07