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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212641Generated: October 25, 2026

Acrylonitrile → 3,5-Bis(trifluoromethyl)cinnamonitrile

https://huagongshe.com/reaction/2212641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
ReactantDi-tert-butylphenylphosphineHCID 316378—
Reactant3,5-Bis(trifluoromethyl)chlorobenzeneHCID 2769405—
Reactantalpha-CyclohexylcyclohexanemethanamineHCID 10774245—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
Product3,5-Bis(trifluoromethyl)cinnamonitrileHCID 273617669%

Reaction Steps

0.382 g (7.2 mmol) of acrylonitrile, 38.7 mg (120 μmol) of NBu4Br, 6.7 mg (30 μmol) of palladium acetate and 26.7 mg (120 μmol) of phenyldi(t-butyl)phosphine are weighed into a Schlenk vessel. 1.49 g (6 mmol) of 3,5-bis(trifluoromethyl)chlorobenzene and 1.53 ml (7.2 mmol) of dicyclohexylmethylamine and also 3.5 ml of dimethylacetamide are then added. The Schlenk vessel is placed in a heating bath at 130° C. and the contents are stirred. After 4 hours, the contents are poured into 30 ml of water and the product is extracted by shaking with t-butyl methyl ether. After drying the organic phase over MgSO4, the solvent is removed under reduced pressure and the product is isolated. Orange oil, yield: 69%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07102046B2
Source datasetuspto-grants-2006_09
ORD IDord-fb848583d510498d9da13547449a7f6e
Source noteuspto-grants-2006_09