HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(3-Acetylureido)-5-phenoxysulfonylnitrobenzene → 2-(3-Acetylureido)-5-phenoxysulfonylaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(3-Acetylureido)-5-phenoxysulfonylnitrobenzene | HCID 15585383 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 2-(3-Acetylureido)-5-phenoxysulfonylaniline | HCID 15585384 | — |
Reaction Steps
48 g of 2-(3-acetylureido)-5-phenoxysulfonylnitrobenzene in 300 ml of methanol and 300 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 dimethylformamide and the solution is evaporated under reduced pressure. The residue is stirred with hot methanol, and the solid is filtered off cold under suction and washed with methanol and diisopropyl ether, melting point 202° C., decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04504490 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-dafcb30e17ad4cb490116da48625e467 |
| Source note | uspto-grants-1985_03 |