HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 13671602, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | 2-Hydroxy-N-(1,2,2,2-tetrachloroethyl)benzamide | HCID 12940170 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13671602 | HCID 13671602 | 71.6% |
Reaction Steps
A solution of N-(1,2,2,2-tetrachloroethyl) salicylamide (30 g) in toluene (100 ml) is added dropwise at less than 10° C. to a solution of 2,2,2-trifluoroethanol (10 g) and pyridine (18.6 g) in toluene (150 ml). After the addition, the mixture is stirred at room temperature for a while, and the contents are washed with water and a 1% aqueous solution of sodium hydrogen carbonate. The toluene layer is dehydrated, and the toluene is evaporated under reduced pressure to give the desired N-[2,2,2,-trichloro-1-(2,2,2,-trifluoroethoxy) ethyl]-salicylamide (26 g) represented by the foregoing formula as a colorless viscous mass. This compound gradually solidifies and shows a melting point of 78° to 82° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04708953 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-98561f82442b4e6c94a4c513c7cfe436 |
| Source note | uspto-grants-1987_11 |