HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441403Generated: October 26, 2026
Potassium Iodide → 1-[gamma-(2-Methyl-4-fluorobenzoyl)-propyl]-4-(3-trifluoromethylphenyl)-4-hydroxypiperidine
https://huagongshe.com/reaction/441403
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-[3-(Trifluoromethyl)phenyl]-4-piperidinol | HCID 75255 | — |
| Reactant | 2-(3-Chloropropyl)-2-(4-fluoro-2-methylphenyl)-1,3-dioxolane | HCID 13002954 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[gamma-(2-Methyl-4-fluorobenzoyl)-propyl]-4-(3-trifluoromethylphenyl)-4-hydroxypiperidine | HCID 13002955 | — |
Reaction Steps
A mixture of 3 g of 4-chloro-1-(2-methyl-4-fluorophenyl)-1,1-ethylenedioxybutane, 2.5 g of 4-(3-trifluoromethylphenyl)-4-hydroxypiperidine, 1,4 g of anhydrous potassium carbonate, 0.05 g of potassium iodide and 30 ml of dimethylformamide was refluxed for 3 hours. The resulting mixture was poured into ice water and was extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate and concentrated in vacuo. To the residual oil were added 60 ml of methanol, 21 ml of water and 10.5 ml of concentrated hydrochloric acid. The mixture was refluxed for 50 minutes and concentrated in vacuo. The residual oil was made alkaline with 28 % aqueous ammonia and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate and concentrated. The residual solid was recrystallized from isopropyl ether to give 1-[γ-(2-methyl-4-flourobenzoyl)-propyl]-4-(3-trifluoromethylphenyl)-4-hydroxypiperidine, melting at about 63.5°-64.5+ C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04039670 |
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| Source dataset | uspto-grants-1977_08 |
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| ORD ID | ord-927041b00c9243889702d8e1c647dfc7 |
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| Source note | uspto-grants-1977_08 |
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