HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Amino-3-nitrobenzophenone → 3,4-Diaminobenzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Amino-3-nitrobenzophenone | HCID 596970 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,4-Diaminobenzophenone | HCID 135520 | 100% |
Reaction Steps
Fifty grams of 4-amino-3-nitrobenzophenone were hydrogenated at room temperature in 945 ml. of tetrahydrofuran with 15 g. of Raney nickel at 2.74×106 dynes/cm.2. After 4 hours three equivalents of hydrogen were absorbed. The catalyst was filtered and the filtrate was evaporated in vacuo to a solid residue. The residue was chromatographed over silica gel using ethyl acetate as eluant. Fractions 5-9 were combined to yield 43.6 g. (100 percent yield) of 3,4-diaminobenzophenone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04174454 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-bd49cab44b95447da5649a4e21c24752 |
| Source note | uspto-grants-1979_11 |