HuagongsheHuagongshe Chemistry Print Report · For research reference only
ethyl 2-(2-nitro-1H-imidazol-1-yl)acetate → 2-(2-Nitroimidazol-1-yl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | ethyl 2-(2-nitro-1H-imidazol-1-yl)acetate | HCID 327541 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-(2-Nitroimidazol-1-yl)acetic acid | HCID 327544 | — |
Reaction Steps
Ethyl 2-(2-nitro-1H-imidazol-1-yl)acetate was suspended in 1N NaOH (100 mL) and stirred at room temperature until it turned into a clear solution. The solution was cooled in an ice-bath and neutralized to pH~2 to give a white precipitate. The solid was filtered and washed with water (3×25 mL). Yield: 11.5 g (97%). MS: 189 (M+NH4)+, 172 (M+H)+, 170 (M-H)-. 1H NMR (DMSO-d6) δ5.22 [s, 2H, C H2 -(2-nitroimidazole)], 7.22 and 7.65 (s, 2H, 2-nitroimidazolyl- H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665329 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-7941eb7e2a7844a0842229ecf5770fb5 |
| Source note | uspto-grants-1997_09 |