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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634120Generated: November 3, 2026

4-Hydroxybenzaldehyde → HCID 12419541, compound

https://huagongshe.com/reaction/1634120

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
Reactant4-BromobutyronitrileHCID 21412—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductHCID 12419541HCID 12419541126.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

4-Hydroxybenzaldehyde (20 mmol) was dissolved in absolute EtOH (150 mL) and treated with solid NaOEt (24 mmol). After stirring for 15 minutes, 4-bromobutyronitrile (24 mmol) was added and reaction mixture was heated overnight at 90° C. in an oil bath. After letting the reaction cool to room temperature, volatiles were removed, the residue was taken up in ice, adjusted to pH 6 with 1N sulfuric acid, and extracted with methylene chloride. The organic phase was washed with brine, dried over MgSO4 and concentrated. Chromatography over silica gel (eluant, 5% EtOAc in hexanes) gave the 4-(3-cyanopropoxy)benzaldehyde (4.8 g, 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506747B1
Source datasetuspto-grants-2003_01
ORD IDord-37895a13fd5144e387b90ba9c93d9f97
Source noteuspto-grants-2003_01