HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-4-nitrobenzene → 4-Nitrodiphenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-4-nitrobenzene | HCID 7474 | — |
| Reactant | Formanilide | HCID 7671 | — |
| Reactant | 55883-46-0 | HCID 86736349 | — |
| Reactant | HCID 86736350 | HCID 86736350 | — |
| Product | 4-Nitrodiphenylamine | HCID 13271 | 93% |
Reaction Steps
Into a suitable reactor is charged 64.4 parts by weight (0.45 mole) of sodium formanilide and 8.0 parts by weight (0.05 mole) of potassium formanilide to give a 90/10 ratio of the salts. In addition, there is added 23.4 parts by weight (0.193 mole) of formanilide and 60.6 parts by weight (0.385) of p-nitrochlorobenzene. The mixture is heated and stirred for 1.5 hours at 152°-160° C. The product is isolated as described in Example 1 to obtain 75.1 parts by weight or 93% yield of 4-nitrodiphenylamine. Conversion of p-nitrochlorobenzene is 98.4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04187249 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-f3cc208d4f4e41c9942b1c7ab590eca0 |
| Source note | uspto-grants-1980_02 |