HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228115Generated: October 30, 2026
Ethanol → 1-(4-(3-(4-Fluoro-phenyl)cinnamoylamino)benzyl)piperidine
https://huagongshe.com/reaction/2228115
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(4-(3-Bromocinnamoylamino)benzyl)piperidine | HCID 53907766 | — |
| Reactant | 4-Fluorophenyl borate | HCID 86756158 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(4-(3-(4-Fluoro-phenyl)cinnamoylamino)benzyl)piperidine | HCID 53967771 | 92.8% |
Reaction Steps
A suspension of 1—(4—(3-bromocinnamoylamino)benzyl)piperidine (0.4 g), 4-fluorophenyl borate (0.14 g), 1M potassium carbonate (2 ml) and ethanol (1 ml) in toluene (5 ml) was stirred under argon atmosphere at room temperature for 30 minutes. To the suspension was added tetrakistriphenylphosphinepalladium (0.05 g), and the mixture was refluxed over night. The mixture was extracted with ethyl acetate, and the organic layer was washed with water and saturated sodium chloride solution, and dried with anhydrous magnesium sulfate. Under reduced pressure, the solvent was evaporated, and the residue was purified with silica gel column (methanol/triethylamine/ethyl. acetate) to give crude crystals, which were recrystallized from ethyl acetate-hexane to give 1—(4—(3—(4-fluoro-phenyl)cinnamoylamino)benzyl)piperidine (Compound 83) (0.35 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06413947B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-7c4380408a6a4b6ba7873b79acb98bac |
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| Source note | uspto-grants-2002_07 |
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