HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120879Generated: October 31, 2026
Trifluoroacetic acid → Piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide
https://huagongshe.com/reaction/2120879
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 4-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester | HCID 12136744 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide | HCID 12020260 | 91.3% |
Reaction Steps
1-(tert-Butoxycarbonyl)-piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide (20) (8.17 g; 17.1 mmol) is dissolved in methylene chloride (60 mL) at ambient temperature. Trifluoroacetic acid (40 mL) is added in a slow stream, and the solution is stirred for 2 hours at ambient temperature. The solution is concentrated in vacuo at 40° C. The residue is dissolved in methylene chloride (400 mL) and poured onto saturated sodium bicarbonate solution. The pH is adjusted to 9 with saturated potassium carbonate solution. The mixture is shaken and the layers separated. The water layer is extracted with methylene chloride (3×100 mL). The combined organic extracts are washed with water, dried over MgSO4, filtered, and concentrated in vacuo affording the desired product (5.91 g) as a white solid. ESMS: MH− 379.0
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06693099B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-367f020176ed491a92bf346ab512174a |
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| Source note | uspto-grants-2004_02 |
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