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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220204Generated: October 27, 2026

Trifluoroacetic acid → (2-Phenyl-piperidin-1-yl)-piperidin-3-yl-methanone

https://huagongshe.com/reaction/220204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3-(2-Phenyl-piperidine-1-carbonyl)-piperidine-1-carboxlic acid tert.-butyl esterHCID 57822310—
SolventDichloromethaneHCID 6344—
Product(2-Phenyl-piperidin-1-yl)-piperidin-3-yl-methanoneHCID 57429185100%

Reaction Steps

To a solution of 1 g 3-(2-phenyl-piperidine-1-carbonyl)-piperidine-1-carboxlic acid tert.-butyl ester in DCM (15 mL) was added 40% trifluoroacetic acid in DCM (6 mL). The mixture was stirred at room temperature for 4-5 h. After completion of the reaction all volatiles were evaporated, water (20 mL) was added and the mixture extracted with (2×25 mL) diethyl ether. The aqueous layer was adjusted with 10% aq. NaOH to pH=12, and extracted with ethyl acetate (2×25 mL). The combined organic layers were dried over sodium sulfate, filtered and evaporated under reduced pressure to yield 0.731 g (95%) of the title compound. (MH+) 273.36.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202888B2
Source datasetuspto-grants-2012_06
ORD IDord-d64216301731458a9006cff360ce50eb
Source noteuspto-grants-2012_06