HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856102Generated: October 29, 2026
Trifluoroacetic acid → 4-[4-(Trifluoromethoxy)phenoxy]piperidine
https://huagongshe.com/reaction/856102
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | tert-Butyl 4-[4-(trifluoromethoxy)phenoxy]piperidine-1-carboxylate | HCID 23081100 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[4-(Trifluoromethoxy)phenoxy]piperidine | HCID 16115439 | 83% |
Reaction Steps
Tert-butyl 4-(4-trifluoromethoxyphenoxy)-piperidine-1-carboxylate (92 g, 254.59 mmol) prepared in Reference Example 189 was dissolved in methylene chloride (100 ml). Trifluoroacetic acid (200 ml) was added dropwise to this solution at room temperature, and the mixture was stirred overnight. The reaction mixture was concentrated under reduced pressure, and the residue was then dissolved in methylene chloride, which was neutralized with a sodium hydroxide aqueous solution. The mixture was extracted with methylene chloride. The extract was washed with brine, dried over sodium sulfate, and then filtered. The filtrate was concentrated under reduced pressure, and the residue was then purified by silica gel column chromatography (methylene chloride/methanol=5/1) to afford 4-(4-trifluoromethoxyphenoxy)piperidine (55 g, yield 83%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262212B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-48601dc8f2c84b50a540aafde8d76560 |
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| Source note | uspto-grants-2007_08 |
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