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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]piperidine-1-carboxylic acid tert-butyl esterHCID 12136765—
SolventDichloromethaneHCID 6344—
Product2-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809093B2
Source datasetuspto-grants-2004_10
ORD IDord-0415e9ef955347998fe479ac027edaf7
Source noteuspto-grants-2004_10