HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-(Benzenesulfinyl)-2-nitroaniline → 4-(Benzenesulfinyl)benzene-1,2-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-(Benzenesulfinyl)-2-nitroaniline | HCID 13035572 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(Benzenesulfinyl)benzene-1,2-diamine | HCID 13035573 | — |
Reaction Steps
5.4 G. of 2-amino-4-phenylsulfinyl-1-nitrobenzen is hydrogenated at 1 atmosphere pressure in 500 ml. methanol in the presence of 5 g. 5% palladized carbon, until the theoretical uptake of hydrogen has occurred. The catalyst is removed by filtration and the filtrate stripped under vacuum. The residue is recrystallized from methanol-benzene, yielding 1,2-diamino-4-phenylsulfinylbenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04011320 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-4f0e5dcf70bb4d97b8a1bcef74d802bb |
| Source note | uspto-grants-1977_03 |