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 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Chlorobenzoyl cyanide | HCID 11984278 | 68% |
Reaction Steps
Metachlorobenzoyl chloride (43.8 g, 0.1 mol), cuprous cyanide (29.1 g, 0.13 mol), and acetonitrile (20 mL) in toluene (37 mL) were refluxed for 3 hours, and were cooled to room temperature. Then, insoluble substances were removed through filtration, and the residue was washed with toluene. Solvent in the resulting filtrate was evaporated under reduced pressure, and the residue was distilled to give metachlorophenyloxoacetonitrile (28 g, 68% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06777224B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-6d9b6352e7d04260a4772070a9eb522c |
| Source note | uspto-grants-2004_08 |