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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380533Generated: October 31, 2026

Ammonium formate → 4-(3-phenyl-2-((S)-2-phenylpropionyl)oxypropyl)piperidine

https://huagongshe.com/reaction/380533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant1-Benzyl-4-(3-phenyl-2-((S)-2-phenylpropionyl)oxypropyl)piperidineHCID 59970767—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product4-(3-phenyl-2-((S)-2-phenylpropionyl)oxypropyl)piperidineHCID 59970765—

Reaction Steps

A solution of 0.310 g (0.7 mmol) of 1-benzyl-4-(3-phenyl-2-((S)-2-phenylpropionyl)oxypropyl)piperidine (Step 1a, isomer 1a), 0.8 g of ammonium formate, and 0.3 g of Pearlman's Catalyst (Pd(OH)2, 20% Pd, moist, Degussa type) in 20 mL of methanol was heated at reflux for 1 h. The mixture was cooled to rt and filtered through a pad of celite and concentrated to afford isomer 1b of the title compound which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06303593B1
Source datasetuspto-grants-2001_10
ORD IDord-7f13b656011640bb9238b44c6a5c82cd
Source noteuspto-grants-2001_10