HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-fluoro-N-(4-nitrophenyl)benzamide → N-(4-Aminophenyl)-4-fluorobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-fluoro-N-(4-nitrophenyl)benzamide | HCID 3948428 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-Aminophenyl)-4-fluorobenzamide | HCID 10988055 | 98.7% |
Reaction Steps
To a solution of 56.6 gm (0.217 mole) 4-(4-fluorobenz-oyl)aminonitrobenzene in 875 mL tetrahydrofuran were added 5.7 gm 5% platinum on carbon. The reaction mixture was hydrogenated at room temperature for 18 hours at initial hydrogen pressure of 60 p.s.i. The reaction mixture was then filtered and the filtrate concentrated under reduced pressure to give 49.3 gm (98.5%) of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05708187 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-ccf2297eda5a41cc90426f03eaece458 |
| Source note | uspto-grants-1998_01 |