HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(3-nitrophenyl)-1H-imidazole → 3-(1H-imidazol-1-yl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(3-nitrophenyl)-1H-imidazole | HCID 817976 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-(1H-imidazol-1-yl)aniline | HCID 321225 | — |
Reaction Steps
To 3-(1-imidazolyl)nitrobenzene (51.6 g, 0.27 mol) in acetic acid (500 ml) is added palladium catalyst (5 g 5% Pd on activated carbon) and the mixture is hydrogenated under pressure (Pstart :4 bar) until the hydrogen uptake has ceased. The mixture is filtered through celite and the filtrate is evaporated to dryness to leave 2d as a light-brown oil. Yield: 40.4 g (93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05922725 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-ddc97b91405f47cfa0eaba1cdc5c1e0d |
| Source note | uspto-grants-1999_07 |