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HRID 898805作成日:2026年10月25日

m-Formylbenzonitrile → 3-Ethenylbenzonitrile

https://huagongshe.com/reaction/898805

反応式

関与物質

役割名称HCID仕込み量
反応物m-FormylbenzonitrileHCID 90670—
反応物ButyllithiumHCID 178418339—
触媒Methyltriphenyliphosphonium bromideHCID 74505—
溶媒TetrahydrofuranHCID 8028—
生成物3-EthenylbenzonitrileHCID 22054362.9%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07351822B2
出典データセットuspto-grants-2008_04
ORD IDord-852856887a6847bb968bb81a98491c1a
出典メモuspto-grants-2008_04