HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496603Generated: October 25, 2026
m-Formylbenzonitrile → 3-Ethenylbenzonitrile
https://huagongshe.com/reaction/496603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Formylbenzonitrile | HCID 90670 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Ethenylbenzonitrile | HCID 220543 | 62.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06946467B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-5319d6c445d948d4b259f206e53fe953 |
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| Source note | uspto-grants-2005_09 |
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