HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorobenzonitrile → 2-(Cyano(4-fluorophenyl)methyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorobenzonitrile | HCID 13391 | — |
| Reactant | Benzeneacetonitrile, 4-fluoro- | HCID 68016 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Cyano(4-fluorophenyl)methyl)benzonitrile | HCID 2773937 | — |
Reaction Steps
To a stirred solution of 700 gr potassium tert-butoxide in 3.6 ltr N,N-dimethylformamide (DMF) is added gradually a solution of 401.4 gr 4-fluorobenzylcyanide and 429.2 gr 2-chlorobenzonitrile in 1.2 ltr DMF, maintaining an internal temperature between 25° C. and 30° C. (ice bath). The reaction mixture is subsequently stirred for one hour at ambient temperature and quenched with dilute hydrochloric acid. Extractive work-up with diethylether gives the product 2-cyano-4'-fluorobenzhydrylcyanide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04873344 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-83b353e67a3e47b9b31a2a139c9fa280 |
| Source note | uspto-grants-1989_10 |