HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2,4-Trichlorobenzene → 2-hydroxy-N-(2-methylphenyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2,4-Trichlorobenzene | HCID 13 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | O-Toluidine | HCID 7242 | — |
| Reactant | Phenyl Salicylate | HCID 8361 | — |
| Product | 2-hydroxy-N-(2-methylphenyl)benzamide | HCID 768318 | 90.2% |
Reaction Steps
Phenol was distilled from a boiling mixture of phenyl salicylate (42.8 gm, 0.20 mol), 2-toluidine (26.7 gm, 0.25 mol), and 1,2,4-trichlorobenzene (41 mL) as described in the literature procedure (Organic Syntheses, Coll. Vol. 3, 765). The cooled product mixture was transferred to an 250 mL Erlenmeyer flask and boiled with hexanes (75 mL) for 30 minutes. The solid product was isolated from the hot mixture by vacuum filtration. The solid was washed with more hexanes until the filtrate was colorless. Drying gave the pure 2′-methyl-salicylanilide (41 gm, 90%) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06664427B1 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-4da7dd80d24f44b69909143c9a0a173e |
| Source note | uspto-grants-2003_12 |