HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha,alpha,alpha-Trifluoro-3-nitro-o-xylene → Trifluoromethyl toluidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha,alpha,alpha-Trifluoro-3-nitro-o-xylene | HCID 81171 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Trifluoromethyl toluidine | HCID 2735932 | 92% |
Reaction Steps
A solution of 2-methyl-3-nitrobenzotrifluoride (41.0 g, 0.2 m) in methanol (100 ml) was stirred under an atmosphere of dry nitrogen at room temperature and palladium on charcoal catalyst (10% w/w, 1.0 g) was added. The stirred mixture was warmed to 40°-45° and then hydrogen was passed into the solution at atmospheric pressure until the reduction, as observed by thin-layer chromatography, was complete (4-5 hours). The solution was cooled to room temperature and the catalyst removed by filtration. Distillation of the solvent at atmospheric pressure followed by steam distillation of the crude product gave 3-amino-2-methylbenzotrifluoride (32.2 g, 92% yield), as a pale-brown oil which slowly crystallized.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04831193 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-09fda287c2444726b8e8807006589159 |
| Source note | uspto-grants-1989_05 |