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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073650Generated: October 31, 2026

Acrylonitrile → HCID 3041687, compound

https://huagongshe.com/reaction/2073650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
ReactantTriethylamineHCID 8471—
Reactant4-Bromobenzoic acidHCID 11464—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantHCID 53717999HCID 53717999—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 3041687HCID 304168735%

Reaction Steps

The 4-chloroformylcinnamonitrile can be prepared as follows: 10.05 g (50 mmols) of 4-bromobenzoic acid, 3.31 g (62.5 mmols) of acrylonitrile, 12.6 g (125 mmols) of triethylamine, 0.112 g (0.5 mmol) of palladium acetate, 0.608 g (2 mmols) of tri-o-tolylphosphine and 20 ml of toluene are boiled under reflux for 6 hours. The reaction mixture is extracted by shaking with 100 ml of 2N hydrochloric acid and the crude product is filtered off and recrystallised from methanol. 3 g (35% of theory) of 4-carboxycinnamonitrile are obtained in the form of pale yellow crystals; melting point 281° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04918215
Source datasetuspto-grants-1990_04
ORD IDord-61d2c50a4f9646b4893d1583f9c07024
Source noteuspto-grants-1990_04