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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720913Generated: October 29, 2026

Trifluoroacetic acid → 1-(Piperidine-4-carbonyl)-piperidine-2-carboxylic acid [4-phenyl-1(3-phenyl-propyl)-butyl]-amide

https://huagongshe.com/reaction/720913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1-(1-Tert-butoxycarbonylpiperidine-4-carbonyl)-piperidine-2 carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 18727503—
SolventDichloromethaneHCID 6344—
Product1-(Piperidine-4-carbonyl)-piperidine-2-carboxylic acid [4-phenyl-1(3-phenyl-propyl)-butyl]-amideHCID 1872749287.2%

Reaction Steps

1-(1-tert-butoxycarbonylpiperidine-4-carbonyl)-piperidine-2-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide (75) (1.41 g; 2.39 mmol) is dissolved in methylene chloride (30 mL) at ambient temperature. Trifluoroacetic acid (15 mL) is added in a slow stream, and the solution is stirred for 2.25 hours at ambient temperature. The solution is concentrated in vacuo at 40° C. The residue is dissolved in methylene chloride (200 mL) and poured onto saturated sodium bicarbonate solution. The pH is adjusted to 9 with saturated potassium carbonate solution. The mixture is shaken the layers separated. The water layer is extracted with methylene chloride (3×50 mL). The combined organic extracts are washed with water, dried over MgSO4, filtered, and concentrated in vacuo affording the desired product (1.02 g) as an oil. ESMS:MH+ 490.4

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135483B2
Source datasetuspto-grants-2006_11
ORD IDord-49a03eda865a4329be54a185f619c4dd
Source noteuspto-grants-2006_11