HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(3-Trifluoromethylphenylsulfonyloxy)-2-ureidonitrobenzene → 5-(3-Trifluoromethylphenylsulfonyloxy)-2-ureidoaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(3-Trifluoromethylphenylsulfonyloxy)-2-ureidonitrobenzene | HCID 15585499 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 5-(3-Trifluoromethylphenylsulfonyloxy)-2-ureidoaniline | HCID 15585470 | — |
Reaction Steps
61.5 g of 5-(3-trifluoromethylphenylsulfonyloxy)-2-ureidonitrobenzene in 200 ml of methanol and 200 ml of 2-methoxyethanol are hydrogenated under normal pressure with a catalytic amount of Raney nickel. After hydrogen uptake is complete, the catalyst is filtered off with suction, washed with methanol and the solution is evaporated under reduced pressure, 1 liter of water is added, and the solid is filtered off with suction, washed with water and dried over NaOH, melting point 172° C., decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04504490 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-1e69c5487f4b416b91c10fc3e96f5f82 |
| Source note | uspto-grants-1985_03 |