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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836081Generated: November 1, 2026

Acetonitrile → 3-Chlorobenzoyl cyanide

https://huagongshe.com/reaction/1836081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantBenzoyl chloride, 3-chloro-HCID 69252—
SolventTolueneHCID 1140—
Product3-Chlorobenzoyl cyanideHCID 1198427868%

Reaction Steps

Metachlorobenzoyl chloride (43.8 g, 0.1 mol), cuprous cyanide (29.1 g, 0.13 mol), and acetonitrile (20 mL) in toluene (37 mL) were refluxed for 3 hours, and were cooled to room temperature. Then, insoluble substances were removed through filtration, and the residue was washed with toluene. Solvent in the resulting filtrate was evaporated under reduced pressure, and the residue was distilled to give metachlorophenyloxoacetonitrile (28 g, 68% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777224B2
Source datasetuspto-grants-2004_08
ORD IDord-6d9b6352e7d04260a4772070a9eb522c
Source noteuspto-grants-2004_08