HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Benzyloxy)-2,3-dinitrobenzene → 3-(Benzyloxy)benzene-1,2-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Benzyloxy)-2,3-dinitrobenzene | HCID 13971358 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | ethanol Raney-nickel | HCID 86745698 | — |
| Product | 3-(Benzyloxy)benzene-1,2-diamine | HCID 4401288 | 102.3% |
Reaction Steps
To a solution of 3-benzyloxy-1,2-dinitrobenzene (2 g, 0.0073 mol) in 300 ml ethanol Raney-nickel (1 g) was added and the mixture was hydrogenated at room temperature and atmospheric pressure until the uptake of hydrogen ceased (30 min). The colourless solution was filtered (celite) and evaporated to dryness in vacuo to give the title compound as an unstable oil (1.6 g) which was used immediately for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05106862 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-c18ccd15a23a4d11834ee6c982afc680 |
| Source note | uspto-grants-1992_04 |