HuagongsheHuagongshe Chemistry Print Report · For research reference only
(o-Chlorophenyl)acetonitrile → HCID 18934784, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (o-Chlorophenyl)acetonitrile | HCID 76112 | — |
| Reactant | N-Bromosuccinamide | HCID 9834204 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18934784 | HCID 18934784 | 66% |
Reaction Steps
To a solution of 2-chlorobenzylcyanide (1.0 g, 6.60 mmol) in CCl4 (25 mL) was added N-bromosuccinamide (1.29 g, 7.26 mmol) and 2,2′-azobis-(2-methylpropionitrile) (0.05 g, 0.33 mmol). The reaction mixture was allowed to reflux for 48 h. The reaction mixture was then diluted with EtOAc (50 mL) and washed with 0.1 M NaOH (50 mL). The organic phase was concentrated to dryness yielding 1.0 g (66%) product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07169777B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-41980cd403e348529b6bf5199b2862b3 |
| Source note | uspto-grants-2007_01 |