HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(3-Acetylureido)-5-(3-trifluoromethylphenylsulfonyloxy)nitrobenzene → 2-(3-Acetylureido)-5-(3-trifluoromethylphenylsulfonyloxy)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(3-Acetylureido)-5-(3-trifluoromethylphenylsulfonyloxy)nitrobenzene | HCID 15585500 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 2-(3-Acetylureido)-5-(3-trifluoromethylphenylsulfonyloxy)aniline | HCID 15585469 | — |
Reaction Steps
59 g of 2-(3-acetylureido)-5-(3-trifluoromethylphenylsulfonyloxy)nitrobenzene 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 warm 2-methoxyethanol and the solution is evaporated under reduced pressure. Water is added to the residue and it is then filtered off with suction, washed with water and dried over sodium hydroxide, melting point 182° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04504490 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-9a3d943268f24b79bb1d5b2dca8f26fe |
| Source note | uspto-grants-1985_03 |