HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 2-chlorobenzoyl cyanide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 2-Chlorobenzoyl chloride | HCID 69110 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-chlorobenzoyl cyanide | HCID 3534944 | 75% |
Reaction Steps
17.5 g (0.1 mol) 2-chlorobenzoyl chloride, 11.65 g (0.13 mol) copper (I) cyanide, and 8 mL of acetonitrile in 15 mL of 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 12.3 g of 2-chlorophenyloxoacetonitrile (yield=75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07250278B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-ab8b138ed2db46d88e4c0677dbe3a6d8 |
| Source note | uspto-grants-2007_07 |