HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484648Generated: October 29, 2026
Toluene → 3-(4-Ethenylphenyl)-2-propenenitrile
https://huagongshe.com/reaction/484648
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | N,N-Dimethylbenzylamine | HCID 7681 | — |
| Reactant | HCID 53717999 | HCID 53717999 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | 3-(4-Ethenylphenyl)-2-propenenitrile | HCID 3018993 | 44% |
Reaction Steps
2.39 g (12.5 mmols) of 4-chloroformylcinnamonitrile, 1.69 g (12.5 mmols) of N-benzyldimethylamine and 0.0280 g (0.125 mmol) of palladium acetate are added under argon to 25 ml of toluene. The reaction mixture is stirred for 4 hours at 140° C. under an ethylene pressure of 10 bar. The mixture is then extracted by shaking at room temperature with 100 ml of 2N HCl and 100 ml of 2N NaOH and is dried over magnesium sulfate. The solution is then evaporated and the residue is chromatographed over silica gel using methylene dichloride as the migrating agent. The yellow oil thus obtained is dissolved in boiling n-pentane. 0.84 g (44% of theory) of 4-vinylcinnamonitrile are formed at -20° C. in the form of white crystals; melting point 45.8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04533505 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-9ec2c50a9216457cbbeb6b05ae117d0b |
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| Source note | uspto-grants-1985_08 |
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