HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 178443473, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2,3-Difluoro-4-hydroxybenzonitrile | HCID 2736978 | — |
| Reactant | HCID 178443472 | HCID 178443472 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178443473 | HCID 178443473 | — |
Reaction Steps
A mixture of 0.1 mol of trans-4-octylcyclohexanecarbonyl chloride (prepared from the carboxylic acid with oxalyl chloride in toluene) and 75 ml of methylene chloride is added to a mixture of 0.1 mol of 2,3-difluoro-4-cyanophenol (prepared according to Example 4), 0.12 mol of pyridine, 10 mmol of 4-N,N-dimethylaminopyridine and 250 ml of methylene chloride. After the mixture has been stirred at room temperature for 10 hours, it is washed with dilute hydrochloric acid, saturated sodium bicarbonate solution and water. Customary working up gives 4-(trans-4-octylcyclohexanecarbonyloxy)-2,3-difluorobenzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05279764 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-e67b9ff39b2e4e4caacb034d196573b9 |
| Source note | uspto-grants-1994_01 |