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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415579Generated: November 2, 2026

Benzene → HCID 21483200, compound

https://huagongshe.com/reaction/1415579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactant1-Chloro-4-nitrobenzeneHCID 7474—
ReactantPotassium HydroxideHCID 14797—
Reactant2,4-DichlorophenylacetonitrileHCID 80566—
SolventPyridineHCID 1049—
ProductHCID 21483200HCID 21483200—

Reaction Conditions

Temperature-5 °C

Reaction Steps

To a solution of 39 parts of potassium hydroxide in 39 parts of pyridine is added a solution of 17 parts of 1-chloro-4-nitrobenzene in 46 parts of pyridine. The whole is cooled to -5° C and there is added dropwise a solution of 22 parts of 2,4-dichlorobenzeneacetonitrile in pyridine, while still cooling at -5° C. Upon completion, stirring is continued for 10 hours at 0° C. After the addition of 90 parts of benzene, the product is precipitated. It is filtered off, washed on the filter with benzene and taken up in water. The aqueous mixture is treated with acetic acid, whereupon the product is separated as an oil. The latter is extracted with methylbenzene. The extract is dried, filtered and evaporated. The residue is crystallized from a mixture of methanol, 2,2' -oxybispropane, petroleumether and trichloromethane, yielding 2,4-dichloro-α-(4-nitrophenyl)benzeneacetonitrile; mp. 81°- 82.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04005218
Source datasetuspto-grants-1977_01
ORD IDord-ea7c520f7e624c129f2231fd3b718341
Source noteuspto-grants-1977_01