HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Fluoro-3-nitrobenzene → HCID 19425982, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Fluoro-3-nitrobenzene | HCID 9823 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178466152 | HCID 178466152 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 19425982 | HCID 19425982 | — |
Reaction Steps
4-Acetylbenzimidazole (4.4 g, 27.5 mmol) was dissolved in dry DMSO (40 ml) and cooled. Sodium hydride (0.91 g, 80% suspension in oil) was added and the mixture was allowed to warm to room temperature. When the evolution of hydrogen had ceased 1-fluoro-3-nitrobenzene was added and the mixture was heated to 120° C. overnight. After cooling the reaction mixture was poured into ice-water and the crude product was filtered off. Purification was achieved by column chromatography on silica gel with ethyl acetate/petroleum ether (1:1) as the eluent. Yield 2.09 g, mp 175°-177° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554630 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-53d9d2567d24473a853f91f496e0c200 |
| Source note | uspto-grants-1996_09 |