HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-methyl-1-(4-nitrobenzyl)-1H-imidazole → 1-(4-aminobenzyl)-5-methyl-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-methyl-1-(4-nitrobenzyl)-1H-imidazole | HCID 426633 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-aminobenzyl)-5-methyl-1H-imidazole | HCID 69208541 | 97% |
Reaction Steps
A mixture of 5-methyl-1-(4-nitrobenzyl)-1H-imidazole (1.4 g), 10% palladium carbon (200 mg) and ethanol (20 ml) was stirred under a hydrogen atmosphere at room temperature for 4 hrs. Palladium carbon was removed from the reaction mixture by filtration, and the filtrate was concentrated. Recrystallization of the residue from ethyl acetate-hexane gave 1-(4-aminobenzyl)-5-methyl-1H-imidazole (1.17 g, 97%) as colorless prism crystals. melting point: 124-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07423159B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-796834830e984f95906c43c487a8bc70 |
| Source note | uspto-grants-2008_09 |