HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4-Ethyl-2-fluoro-N-(2-hydroxyphenyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Aminophenol | HCID 5801 | — |
| Reactant | 4-Ethyl-2-fluorobenzoyl chloride | HCID 21413837 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-Ethyl-2-fluoro-N-(2-hydroxyphenyl)benzamide | HCID 21413807 | — |
Reaction Steps
To a solution of 13.08 gm. of o-aminophenol in 150 cc. of dry pyridine which is cooled in ice water is added a solution of 4-ethyl-2-fluorobenzoyl chloride (prepared from 20.0 gm. of acid and thionyl chloride) in 30 cc. of dry benzene. The mixture is stirred at room temperature overnight and then concentrated in vacuo. The residue is treated with water and the precipitate collected by filtration to give crude 4-ethyl-2-fluoro-2'-hydroxybenzanilide which was characterized by infra red spectra then used in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03947582 |
| Source dataset | uspto-grants-1976_03 |
| ORD ID | ord-a5b5cc4344694a73aff36ec7f2caacf3 |
| Source note | uspto-grants-1976_03 |