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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108716Generated: October 30, 2026

Methyl 3-(3-(N-Boc-piperidin-4-yl)-propoxy)-phenylacetate → 3-(3-(N-Boc-piperidin-4-yl)-propoxy)-phenylacetic acid

https://huagongshe.com/reaction/2108716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-(3-(N-Boc-piperidin-4-yl)-propoxy)-phenylacetateHCID 21071299—
SolventMethanolHCID 887—
Product3-(3-(N-Boc-piperidin-4-yl)-propoxy)-phenylacetic acidHCID 21071295—

Reaction Conditions

Temperature60 °C

Reaction Steps

Methyl 3-(3-(N-Boc-piperidin-4-yl)-propoxy)-phenylacetate (0.5 g, 1.3 mmol) was dissolved in methanol, and 2N NaoH (3 mL) added. The reaction was stirred at 60° C. for 2 h, then the solution was adjusted to pH 6.5, the product was extracted into ethyl acetate and the organic phase was dried by MgSO4. Removal of solvent revealed 3-(3-(N-Boc-piperidin-4-yl)-propoxy)-phenylacetic acid (0.30 g). 1H NMR (500 MHz, CDCl3) δ 1.02 (m, 2H), 1.25 (m, 2H), 1.55 (m, 2H), 1.65 (m, 2H), 2.57 (m, 2H), 3.33 (m, 1H), 3.75 (s, 2H), 3.95 (m, 2H), 6.63 (m, 3H), 6.98 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514448B2
Source datasetuspto-grants-2009_04
ORD IDord-da2768b61dbe45e691c31178aec27fab
Source noteuspto-grants-2009_04