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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701928Generated: October 30, 2026

Acrylonitrile → alpha,4-Dichloro-2-(benzoyl)benzenepropanenitrile

https://huagongshe.com/reaction/1701928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
ReactantTert-Butyl nitriteHCID 10906—
Reactant2-Amino-5-chlorobenzophenoneHCID 12870—
Reactant2,5-DichlorobenzophenoneHCID 458188—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
Productalpha,4-Dichloro-2-(benzoyl)benzenepropanenitrileHCID 13067144—

Reaction Steps

A solution of 92.7 g (0.4 mole) of 2-amino-5-chlorobenzophenone in 250 ml of acetonitrile was added to a mixture of 70 g (0.52 mole) of cupric chloride, 65 g (0.63 mole) of t-butylnitrite, 500 ml of acrylonitrile, and 500 ml of acetonitrile. When the addition was complete stirring at room temperature was continued for 2 hr. The mixture was diluted with 80 ml of 6 N hydrochloric acid and 1500 ml of water, extracted with ether and dried over anhydrous sodium sulfate. The ether solution was concentrated at reduced pressure to give a brown oil, which contained the end product and 2,5-dichlorobenzophenone. Trituration of the oil with a mixture of ether and petroleum ether gave the end product as a tan solid. Recrystallization of a small portion of the end product from a mixture of ether and petroleum ether gave pale yellow needles, mp 69°-71°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04379765
Source datasetuspto-grants-1983_04
ORD IDord-a24c7f74da174119bdd4bb3d0ac64872
Source noteuspto-grants-1983_04