HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393992Generated: October 29, 2026
Trifluoroacetic acid → 2-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidine
https://huagongshe.com/reaction/393992
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]piperidine-1-carboxylic acid tert-butyl ester | HCID 12136765 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidine | HCID 12992460 | — |
Reaction Steps
1-(tert-Butoxycarbonyl)-piperidine-2-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide (30) (6.77 g; 14.1 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 1.25 hours at ambient temperature. The solution is concentrated in vacuo at 40° C. The residue is dissolved in methylene chloride (300 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 as a solid. ESMS: MH+ 379.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06809093B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-0415e9ef955347998fe479ac027edaf7 |
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| Source note | uspto-grants-2004_10 |
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