HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Salicylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trichloroethanol | HCID 8259 | — |
| Reactant | 2-Hydroxy-N-(1,2,2,2-tetrachloroethyl)benzamide | HCID 12940170 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Salicylamide | HCID 5147 | 272.5% |
Reaction Steps
A solution composed of 2,2,2-trichloroethanol (30 g), N-(1,2,2,2-tetrachloroethyl) salicylamide (30 g) and toluene (200 ml) is refluxed until the generation of hydrogen chloride ceases (for about 5 to 8 hours). The reaction mixture is cooled to room temperature. The toluene layer is washed with water and dehydrated, and toluene is evaporated under reduced pressure to give the desired N-8 2,2,2-trichloro-1-(2,2,2-trichloroethoxy)-ethyl]salicylamide (37 g) represented by the foregoing formula as colorless crystals. mp. 111°-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04708953 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-3e5b45c45a7c44ce86cd38507e1e61de |
| Source note | uspto-grants-1987_11 |