HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(4-Fluorobenzoyl)-1-(4-nitrobenzoyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | p-Fluorophenyl 4-piperidyl ketone hydrochloride | HCID 3084438 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Fluorobenzoyl)-1-(4-nitrobenzoyl)piperidine | HCID 13603965 | 85.5% |
Reaction Steps
4-Nitrobenzoyl chloride (3.08 g) was added slowly to a stirred mixture of 4-(4-fluorobenzoyl)piperidine hydrochloride (4.0 g) and triethylamine (4.98 g) in methylene chloride (110 ml) at room temperature. The resulting mixture was stirred at this temperature for 1 hour, washed with 1N hydrochloric acid, saturated sodium bicarbonate solution, and brine, dried over magnesiun sulfate and concentrated in vacuo. The residue was recrystallized from a mixture of acetone and methanol to give 4-(4-fluorobenzoyl)-1-(4-nitrobenzoyl)piperidine (5.0 g) as colourless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04735952 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-62f909a151c64ea7bb61e29664fb3cbd |
| Source note | uspto-grants-1988_04 |