HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromo-2-nitrobenzene-1-thiol → 2-amino-4-bromobenzene-1-thiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromo-2-nitrobenzene-1-thiol | HCID 21980019 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-amino-4-bromobenzene-1-thiol | HCID 12199294 | — |
Reaction Steps
The mixture of 4-bromo-2-nitro-benzenethiol and its disulfide from Example 2A (14.9 g, 53.5 mmol) in THF (450 mL) was mixed with Raney Ni (30 g, 100% wt). The mixture was hydrogenated in a 1000 mL Paar shaker at a hydrogen pressure of 40 psi at 50° C. for 41 hours. When the reaction was complete, the solids were filtered. The solid filter-cake was dissolved in pyridine (600 mL) at 100° C. and filtered to remove the Ni residue. This pyridine solution contained mostly the 2-amino-4-bromophenyldisulfide. Crude yield=11.9 g (92%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106088B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-2513e554b3aa42558ab50fb69c2471cc |
| Source note | uspto-grants-2012_01 |