HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3,4-Trifluoro-1-nitro-5-(trifluoromethyl)benzene → HCID 15614237, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3,4-Trifluoro-1-nitro-5-(trifluoromethyl)benzene | HCID 15614236 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15614237 | HCID 15614237 | 87.9% |
Reaction Steps
35 g of 2,3,4-trifluoro-5-nitro-benzotrifluoride in 150 ml of tetrahydrofuran were initially introduced into a hydrogenation apparatus, 3 g of Raney nickel were added and, after flushing with nitrogen, the mixture was hydrogenated to constant pressure with 30 bar of hydrogen at 25° to 45° C. After completion of the hydrogen uptake, the pressure was released and the reaction solution was filtered and subsequently fractionally distilled. 27 g of 2,3,4-trifluoro-5-amino-benzotrifluoride were obtained with a boiling point of 82° to 83° C. at 15 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05082971 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-2cdd080e605843298aca1d905ea8d5da |
| Source note | uspto-grants-1992_01 |