HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537204Generated: October 25, 2026
Potassium Carbonate → 4-(4-Chlorophenyl)-1-(3,3-diphenyl-propyl)-4-fluoropiperidine
https://huagongshe.com/reaction/537204
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,3-Diphenylpropyl iodide | HCID 15512878 | — |
| Reactant | 4-(4-Chlorophenyl)-4-fluoropiperidine hydrochloride | HCID 67464633 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Chlorophenyl)-1-(3,3-diphenyl-propyl)-4-fluoropiperidine | HCID 67462709 | — |
Reaction Steps
A solution of 4-(4-chlorophenyl)-4-fluoropiperidine hydrochloride (100 mg, 0.40 mmol) and 3,3-diphenyl-1-iodopropane (145 mg, 0.45 mmol) in DMF (2.5 mL) was treated with potassium carbonate (560 mg, 4.05 mmol) and the resulting suspension heated at 80° C. for 14 hours. After this time the reaction was cooled to room temperature and quenched by pouring into 25% aqueous ammonium chloride solution (20 mL). The resulting suspension was then extracted with ethyl acetate (2×10 mL) and the combined extracts washed with water (10 mL) and brine (10 mL) then dried over magnesium sulfate. Subsequent filtration and concentration under reduced pressure afforded crude 4-(4-chlorophenyl)-1-(3,3-diphenyl-propyl)-4-fluoropiperidine as a yellow oil. This material was treated with 10% methanolic hydrogen chloride (10 mL) and the solution concentrated under reduced pressure. Trituration of the resulting oil with 1:1 ethyl acetate/2-butanone (10 mL) afforded a solid which was isolated by filtration and vacuum dried. This afforded a 41% yield of 4-(4-chlorophenyl)-1-(3,3-diphenylpropyl)-4-fluoropiperidine hydrochloride as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859777B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-dc7a507a742d4592a8486e6fa6270869 |
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| Source note | uspto-grants-2014_10 |
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