HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 14439311, compound → 2,4-Difluoro-5-(trifluoromethoxy)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 14439311 | HCID 14439311 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,4-Difluoro-5-(trifluoromethoxy)aniline | HCID 14439312 | 80.3% |
Reaction Steps
In a hydrogenation apparatus, 27 g of 3-nitro-4,6-difluoro-trifluoromethoxy-benzene in 150 ml of tetrahydrofuran are hydrogenated at 30 to 50 bar hydrogen at 25° to 45° C., in the presence of 3 g of Raney nickel. When the hydrogen uptake is complete, the mixture is filtered, and the filtrate is distilled. 19 g of 3-amino-4,6-difluoro-trifluoromethoxy-benzene of a boiling point of 82° to 83° C. at 20 mbar are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04952601 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-93a40823a6b046beafa235e4dd73ff22 |
| Source note | uspto-grants-1990_08 |