HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193675Generated: October 31, 2026
Potassium Iodide → 4-[Bis(4-fluorophenyl)methyl]-1-[3-(3,5-dimethoxyphenoxy)propyl]piperidine
https://huagongshe.com/reaction/1193675
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-[Bis(4-fluorophenyl)methyl]piperidine | HCID 13250544 | — |
| Reactant | 1-(3-Chloropropoxy)-3,5-dimethoxybenzene | HCID 14407174 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Ethyl acetate dimethoxyethane | HCID 87198031 | — |
| Product | 4-[Bis(4-fluorophenyl)methyl]-1-[3-(3,5-dimethoxyphenoxy)propyl]piperidine | HCID 14407094 | — |
Reaction Steps
A mixture of 5.51 g (0.019 mole) of 4-[bis(4-fluorophenyl)methyl]piperidine, 4.42 g (0.019 mole) of 1-(3-chloropropoxy)-3,5-dimethoxybenzene and potassium carbonate (5.53 g, 0.04 mole) was heated overnight at reflux in 350 ml of 1-butanol containing potassium iodide (0.3 g). The reaction mixture was stripped to dryness and the residue partitioned between chloroform-5% sodium hydroxide and chloroform-water. Removal of chloroform gave a brown oil. The oil was subjected to chromatography on a silica gel column using a gradient elution series of hexane-ethyl acetate and ethyl acetate-dimethoxyethane. After combining proper fractions eluted from the column and removing solvent, the residual oil was dried in vacuo overnight at 80° C. This produced 2.61 g (28.5%) of brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04810713 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-c3ca385633b04030a9eae1086601ef75 |
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| Source note | uspto-grants-1989_03 |
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