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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393977Generated: October 27, 2026

Trifluoroacetic acid → Piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide

https://huagongshe.com/reaction/393977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 12136744—
SolventDichloromethaneHCID 6344—
ProductPiperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 1202026095.2%

Reaction Steps

4-[4-Phenyl-1-(3-phenyl-propyl)-butylcarbamoyl]-piperidine-1-carboxylic acid tert-butyl ester (3) (0.77 g; 1.61 mmol) is dissolved in methylene chloride (20 mL) at ambient temperature. Trifluoroacetic acid (20 mL) is added in a slow stream, and the solution is stirred for 90 minutes at ambient temperature. The solution is concentrated in vacuo at 40° C. The residue is slurried in a mixture of methylene chloride (10 mL) and water (100 mL), then potassium carbonate is added until the slurry is alkaline. The slurry is diluted with water (200 mL) then extracted with methylene chloride (3×100 mL). The organic extracts are dried over MgSO4, filtered, and concentrated in vacuo affording the desired product (0.58 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809093B2
Source datasetuspto-grants-2004_10
ORD IDord-3c9a176da4614da5b649eecb780d5a7f
Source noteuspto-grants-2004_10