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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1826595Erstellt: 25. Oktober 2026

m-Formylbenzonitrile → 3-Ethenylbenzonitrile

https://huagongshe.com/reaction/1826595

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktm-FormylbenzonitrileHCID 90670—
EduktButyllithiumHCID 178418339—
KatalysatorMethyltriphenyliphosphonium bromideHCID 74505—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-EthenylbenzonitrileHCID 22054362,9%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07053078B2
Quelldatensatzuspto-grants-2006_05
ORD IDord-0a2510e73c644802b9286dd90eeea400
Quellennotizuspto-grants-2006_05