HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyanophenol → 4-((5-Chloropentyl)oxy)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Bromo-5-chloropentane | HCID 96070 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-((5-Chloropentyl)oxy)benzonitrile | HCID 19381510 | — |
Reaction Steps
To a solution of 16.9 g (135 mmol) p-cyanophenol in 169 mL of dimethylformamide (DMF), cooled in an ice-bath is added in portions 6.5 g (135 mmol) sodium hydride (50% dispersion in oil). The reaction is stirred and allowed to warm-up to room temperature until no further hydrogen evolution is observed. The solution is then cooled in an ice-bath and a solution of 1-bromo-5-chloro-pentane 25 g (135 mmol) in 84 mL of dimethylformamide is added. The reaction is allowed to warm up to room temperature and stirred for 18 h. The reaction is then poured onto water and the resulting solid filtered off and dried to give 4-(5-chloropentoxy) benzonitrile, m.p. 52°-54° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05246965 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-47bbd098cb2a4725a243aeb6e8e75282 |
| Source note | uspto-grants-1993_09 |