Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-[Bis(4-fluorophenyl)methyl]piperidine | HCID 13250544 | — |
| Reactant | HCID 14407179 | HCID 14407179 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 23036460 | HCID 23036460 | 50.1% |
Reaction Steps
A mixture of 6.02 g (0.021 mole) of 4-[bis(4-fluorophenyl)methyl]piperidine and 5.22 g (0.021 mole) of 1-(3-chloropropoxy)-4-(methylsulfonyl)benzene in 350 ml of 1-butanol containing potassium carbonate (5.53 g, 0.04 mole) and potassium iodide (0.2 g) was heated overnight at gentle reflux. The reaction was filtered and stripped to dryness. The residue obtained was dissolved in chloroform and extracted with water. The chloroform layer was dried, filtered, and solvent removed to give an oil. The dark brown oil was converted to the oxalate salt and recrystallized from methanol-diethyl ether to give a white solid. This material was dried in vacuo overnight at 65° C. A yield of 6.21 g (50.1%) of white crystalline solid, m.p. 202°-204° C. was obtained.
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-1526aa157f394c8285cf21638e756c0e |
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| Source note | uspto-grants-1989_03 |
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