HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 3-Chlorobenzoyl cyanide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Benzoyl chloride, 3-chloro- | HCID 69252 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Chlorobenzoyl cyanide | HCID 11984278 | 169.1% |
Reaction Steps
43.8 g (0.1 mol) 3-chlorobenzoyl chloride, 29.1 g (0.13 mol) copper (I) cyanide, and 20 mL acetonitrile in 37 mL toluene was refluxed for 3 hours, and then cooled to room temperature. Insoluble material was filtered and the residue was washed with toluene. The solvent in the resulting filtrate was evaporated under reduced pressure, and the residue was distilled to yield 28 g 3-chlorophenyloxoacetonitrile (yield=68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07250278B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-277e3dda00e143e4bd1664cf26cbe709 |
| Source note | uspto-grants-2007_07 |