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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016538Generated: October 27, 2026

Hydrochloric Acid → 2-Chloro-2-(4-phenoxyphenyl)propionitrile

https://huagongshe.com/reaction/1016538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant2-(4-Phenoxyphenyl)-1-phenyl-1-ethanoneHCID 2824056—
CatalystMagnesium diiodideHCID 5462737—
SolventDichloromethaneHCID 6344—
Product2-Chloro-2-(4-phenoxyphenyl)propionitrileHCID 12056390—

Reaction Steps

A mixture of 4-phenoxyphenylacetophenone (6.36 g), trimethylsilylcyanide (3.96 g) and magnesium iodide (10 mg) in methylene chloride (30 ml) was stirred for 12 hrs at room temperature, 156 hydrochloric acid (10 ml) was then added. The mixture was again stirred for 8 hrs at room temperature. The organic layer was separated and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure. The residue was dissolved in benzene (50 ml) and pyridine (2.37 g) and thionyl chloride (4.76 g) were added at 0° C. with stirring. The reaction mixture was stirred for an additional 3 hrs at room temperature and then the solvent was evaporated. The residue was purified by column chromatography to give 7.09 g of 2-chloro-2-(4-phenoxyphenyl)propionitrile as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476055B1
Source datasetuspto-grants-2002_11
ORD IDord-767406a608fd48ce9617e3ef0ada1853
Source noteuspto-grants-2002_11