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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462641Generated: November 1, 2026

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

https://huagongshe.com/reaction/1462641

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 6N 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 numberUS04460781
Source datasetuspto-grants-1984_07
ORD IDord-b1fc43d430d74d2fa44353e7524539c1
Source noteuspto-grants-1984_07