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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518933Generated: October 30, 2026

Trifluoroacetic acid → HCID 131733365, compound

https://huagongshe.com/reaction/518933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant2-Hydroxy-1-(piperidin-1-yl)ethan-1-oneHCID 6480489—
ReactantHCID 131733364HCID 131733364—
SolventTolueneHCID 1140—
ProductHCID 131733365HCID 131733365—

Reaction Conditions

Temperature50 °C

Reaction Steps

The compound of Step D (3.0 g, 2.9 mmol) is dissolved in 100 mL of toluene. 1.53 g (5.8 mmol) of triphenylphosphine and 0.62 g (4.3 mmol) of 2-hydroxy-1-(1-piperidyl)ethanone are added thereto. The mixture is heated to 50° C., and then 1.01 g (4.3 mmol) of di-tert-butyl azodicarboxylate are added. The reaction mixture is stirred at 50° C. for 1 hour and is then allowed to return to ambient temperature before adding 1 mL of trifluoroacetic acid. After stirring overnight at ambient temperature, the mixture is successively washed with water, saturated NaHCO3 and brine solution. The combined aqueous phases are extracted with ethyl acetate. The resulting organic phases are dried over sodium sulphate, filtered and concentrated under reduced pressure. The crude product obtained is purified by chromatography over silica gel (dichloromethane/ethanol 98/2) to yield the expected compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115159B2
Source datasetuspto-grants-2015_08
ORD IDord-346dae02969e4883a7aab675b3feca46
Source noteuspto-grants-2015_08