Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800823Generated: October 25, 2026

Sodium Cyanide → Benzeneacetonitrile, 2,3-dichloro-

https://huagongshe.com/reaction/1800823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
ReactantDichlorobenzyl chlorideHCID 76790—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductBenzeneacetonitrile, 2,3-dichloro-HCID 229020—

Reaction Steps

2,3-Dichlorobenzylchloride (5.0 g, 25.5 mmol) was dissolved in 100 ml DMSO. 9.2 g NaCN (188 mmol) were added and the mixture stirred at room temperature for 16 hours. The reaction mixture was diluted with water, and the product extracted with ether. The organic layers were washed with water (2×) and brine, then dried over magnesium sulfate, filtered and concentrated. The product was used as. Crude yield˜quantitative. An analytical sample was purified by column chromatography on silica, using a gradient from 10% to 75% dichloromethane in hexanes as eluent. The combined aqueous layers and wash liquids were treated with 100 ml bleach to oxidize the excess cyanide to less toxic materials.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343999B2
Source datasetuspto-grants-2013_01
ORD IDord-95132224f2204bf5be33c7423de2b104
Source noteuspto-grants-2013_01