Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156450Generated: October 31, 2026

Benzoyl chloride → 3-Phenylprop-2-enenitrile

https://huagongshe.com/reaction/1156450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTributylamineHCID 7622—
ReactantAcrylonitrileHCID 7855—
Catalystpalladium(II) acetateHCID 167845—
SolventP-XyleneHCID 7809—
Product3-Phenylprop-2-enenitrileHCID 74667540%

Reaction Steps

The procedure described in Example 1 is repeated, except that 3.31 g (0.0625 mol) of acrylonitrile, 7.02 g (0.05 mol) of benzoyl chloride, 11.6 g (0.0625 mol) of tri-n-butylamine, 100 ml of p-xylene and 0.1122 g (0.0005 mol) of palladium acetate are used. After a reaction time of 2 hours at 120° C., 3.47 g (0.27 mol) of cinnamonitrile are obtained, corresponding to a yield of 54% of theory. Boiling point=134°-136° C./17×102Pa.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04335054
Source datasetuspto-grants-1982_06
ORD IDord-dd8e624985df4102b6c11f4fa8efe689
Source noteuspto-grants-1982_06