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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48131Generated: October 25, 2026

Benzoic acid 1-cyano-3-(4-methoxyphenyl)-allyl ester → 4-(4-Methoxyphenyl)but-3-enenitrile

https://huagongshe.com/reaction/48131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic acid 1-cyano-3-(4-methoxyphenyl)-allyl esterHCID 54392804—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Methoxyphenyl)but-3-enenitrileHCID 5443519957%

Reaction Steps

Benzoic acid 1-cyano-3-(4-methoxy-phenyl)-allyl ester (15 g; ca 0.050 mol) is dissolved in 100 ml of anhydrous tetrahydrofuran. Tetrakis(triphenylphosphine)palladium (0.88 g; 0.8 mmol) and 4.8 ml of poly(methylhydrosiloxane) (ca 80 meq; Aldrich) are added, and the mixture is stirred at ca 20° C., cooling with a cold water bath. After 3 h 30 min, the mixture is concentrated by rotary evaporation, stirred with 150 ml of water to hydrolyze the siloxane. The polymer and organic materials are redissolved in CH2Cl2 and washed with saturated sodium bicarbonate to remove benzoic acid. Evaporation of the solvent and flash chromatography (150 g SiO2; hexane:ethyl acetate 80:20 v:v) affords 4.9 g (57%) of pure 4-(4-methoxy-phenyl)-but-3-enenitrile, mp 75-76° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06703182B1
Source datasetuspto-grants-2004_03
ORD IDord-0ab9cabf15834044aea6d28280ea2ec8
Source noteuspto-grants-2004_03