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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815060Generated: October 25, 2026

m-Formylbenzonitrile → 3-Ethenylbenzonitrile

https://huagongshe.com/reaction/1815060

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-FormylbenzonitrileHCID 90670—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
Product3-EthenylbenzonitrileHCID 22054362.9%

Reaction Steps

To a stirred suspension of methyltriphenylphosphonium bromide (75 g, 209.71 mmol) in dry THF (750 mL) at 0° C. under nitrogen was added dropwise n-BuLi (83 mL, 2.5 M in hexanes, 207.50 mmol). The mixture was warmed to room temperature. 3-Cyanobenzaldehyde (25 g, 190.65 mmol) was added as a solid in 5 g batches, and the mixture was stirred at room temperature overnight. The reaction was quenched in water, and the solvent was removed under vacuum. The residue was dissolved in the minimal amount of THF, and triphenylphosphine oxide was precipitated using ether. The solid was filtered through diatomaceous earth, and the filtrate was concentrated. Distillation by Kugelrhor at 90° C./33 Pa (0.25 mm Hg) gave the product as a colorless oil (15.5 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878725B2
Source datasetuspto-grants-2005_04
ORD IDord-2e33ff17b940480190c71f335273b94f
Source noteuspto-grants-2005_04