HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(1-benzoylpiperidin-4-yl)-4-fluorobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 4-fluoro-N-(piperidin-4-yl)benzamide | HCID 4778226 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1-benzoylpiperidin-4-yl)-4-fluorobenzamide | HCID 9797409 | — |
Reaction Steps
To a suspension of N-(piperidin-4-yl)-4-fluorobenzamide (0.5 g) in dichloromethane (5 ml) were added pyridine (218 μl), dichloromethane (5 ml) and benzoyl chloride (290 μl) at ambient temperature. After stirring for 3.5 hours, water (5 ml) was poured into the mixture. An organic layer was separated, and washed with water and brine. After drying with magnesium sulfate, the solvents were removed under reduced pressure. A residue was purified by column chromatography (silica gel, toluene:ethyl acetate=1:1 to ethyl acetate). After rinse with diisopropyl ether, N-(1-benzoylpiperidin-4-yl)-4-fluorobenzamide (515 mg) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06710043B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-64d0f593fc724881840098bfc8140046 |
| Source note | uspto-grants-2004_03 |