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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388889Generated: October 26, 2026

(R)-((S)-1-phenylethyl)2-(2-fluorophenyl)-2-(piperidin-1-yl)acetate → (R)-2-(2-fluorophenyl)-2-(piperidin-1-yl)acetic acid

https://huagongshe.com/reaction/388889

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-((S)-1-phenylethyl)2-(2-fluorophenyl)-2-(piperidin-1-yl)acetateHCID 59166523—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Product(R)-2-(2-fluorophenyl)-2-(piperidin-1-yl)acetic acidHCID 2732696598.1%

Reaction Steps

A mixture of (R)—((S)-1-phenylethyl) 2-(2-fluorophenyl)-2-(piperidin-1-yl)acetate (0.737 g, 2.16 mmol) and 20% Pd(OH)2/C (0.070 g) in ethanol (30 mL) was hydrogenated at room temperature and atmospheric pressure (H2 balloon) for 2 hours. The solution was then purged with Ar, filtered through diatomaceous earth (CELITE®), and concentrated in vacuo. This provided the title compound as a colorless solid (0.503 g, 98%). 1H NMR (400 MHz, CD3OD) δ 7.65 (ddd, J=9.1, 7.6, 1.5 Hz, 1H), 7.47-7.53 (m, 1H), 7.21-7.30 (m, 2H), 3.07-3.13 (m, 4H), 1.84 (br s, 4H), 1.62 (br s, 2H). LC-MS: Anal. Calcd. for C13H16FNO2: 237. found: 238 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377980B2
Source datasetuspto-grants-2013_02
ORD IDord-4c27d07d049e47ddb60bc8ea87cdac7c
Source noteuspto-grants-2013_02