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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 2-(4-Phenoxyphenyl)-1-phenyl-1-ethanone | HCID 2824056 | — |
| Catalyst | Magnesium diiodide | HCID 5462737 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-2-(4-phenoxyphenyl)propionitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06476055B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-767406a608fd48ce9617e3ef0ada1853 |
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| Source note | uspto-grants-2002_11 |
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