HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → 2-Phenylbut-3-enenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Benzene, 1-(chloromethyl)-3(or 4)-ethenyl- | HCID 11768772 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | 2-Phenylbut-3-enenitrile | HCID 14767509 | 71% |
Reaction Steps
12.2 g of commercially available vinylbenzyl chloride (a mixture of 60% of a meta-isomer and 40% of a para-isomer) were reacted with 5 g of NaCN in a mixed solvent of methanol/water=12.2 g/5 g at 64° C. for 12 hours. A reaction product solution was filtered, and the solvent was then distilled off, followed by distillation under reduced pressure, thereby obtaining 8.1 g of vinylbenzyl cyanide (yield 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05336725 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-a61aa2b44e454a1e831b5e9f53cd3be7 |
| Source note | uspto-grants-1994_08 |