HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 4-Piperidino-5,7-dinitro-2-trifluoromethylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chloro-5,7-dinitro-2-trifluoromethylbenzimidazole | HCID 135677577 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-Piperidino-5,7-dinitro-2-trifluoromethylbenzimidazole | HCID 21489357 | — |
Reaction Steps
Triethylamine (1.0 gram; 0.00968 mole) was added to 3.0 grams of 4-chloro-5,7-dinitro-2-trifluoromethylbenzimidazole (0.00968 mole) in 200 milliliters of benzene. There was then added dropwise 0.8 gram of piperidine (0.00968 mole) in 10 milliliters of benzene. The resulting reaction mixture was refluxed overnight, cooled, an amount of ether added, and the mixture filtered. The filtrate was evaporated, yielding the desired 4-piperidino-5,7-dinitro-2-trifluoromethylbenzimidazole product as an orange solid. It was recrystallized from benzene as a light brown solid, m.p., 199°-206° C. NMR analysis confirmed the identity but suggested the presence of a small amount of triethylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04000295 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-be9073c9e7ab4bdb88a52d8dc1733f8b |
| Source note | uspto-grants-1976_12 |