HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642027Generated: October 31, 2026
Trifluoroacetic acid → 4-{Bis[4-(trifluoromethoxy)phenyl]methyl}piperidin-4-ol
https://huagongshe.com/reaction/1642027
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl 4-{bis[4-(trifluoromethoxy)phenyl]methyl}-4-hydroxypiperidine carboxylate | HCID 86633668 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-{Bis[4-(trifluoromethoxy)phenyl]methyl}piperidin-4-ol | HCID 16656274 | — |
Reaction Steps
A mixture of 3.0 grams (0.0057 mole) of tert-butyl 4-{bis[4-(trifluoromethoxy)phenyl]methyl}-4-hydroxypiperidine carboxylate and 25 mL of methylene chloride was chilled in a wet ice bath. A solution of 2.63 mL trifluoro acetic acid and 5 mL methylene chloride was added dropwise to the reaction mixture during a 5-minute period. The wet ice bath was removed and the reaction mixture was allowed to warm to ambient temperature. The reaction mixture was then warmed to reflux, and allowed to cool to ambient temperature. The reaction mixture was concentrated under reduced pressure. The residue can then be dissolved in 100 mL methylene chloride and reacted with 200 mL of an aqueous solution saturated with sodium carbonate. The methylene chloride layer can then be separated, dried over magnesium sulfate, filtered and concentrated under reduced pressure to yield the subject compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119563B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-a67177cedbe745cd9217d351e96e9391 |
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| Source note | uspto-grants-2012_02 |
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