HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(2,2,2-trifluoro)ethyl-2-(4-nitro-1H-imidazol-1-yl)octanoamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2,2-Trifluoroethylamine hydrochloride | HCID 9772 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-(4-nitro-1H-imidazol-1-yl)octanoic acid | HCID 10083686 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2,2,2-trifluoro)ethyl-2-(4-nitro-1H-imidazol-1-yl)octanoamide | HCID 15222341 | 22.9% |
Reaction Steps
2-(4-Nitro-1H-imidazol-1-yl)octanoic acid (7.8 mmoles,2.0 g) was treated with 25 ml oxalyl chloride, concentrated and added to a solution of trifluoroethylamine hydrochloride (7.8 mmoles, 1.06 g) and triethylamine (2 ml) in 50 ml THF. After stirring at room temperature for 16 hours, the mixture was added to ice, extracted with ethyl acetate, dried over sodium sulfate, and concentrated. The intermediate was chromatographed over silica gel to yield 0.6 g of N-(2,2,2-trifluoro)ethyl-2-(4-nitro-1H-imidazol-1-yl)octanoamide. (MS).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05484780 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-233f3d3d294447f88067464e0e95f6fb |
| Source note | uspto-grants-1996_01 |