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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269503Generated: October 30, 2026

2-(3-{1-[(4-Isopropyl-phenoxy)-acetyl]-piperidin-3-yl}-phenoxy)-2-methyl-propionic acid benzyl ester → 2-(3-{1-[(4-Isopropyl-phenoxy)-acetyl]-piperidin-3-yl}-phenoxy)-2-methyl-propionic acid

https://huagongshe.com/reaction/1269503

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-{1-[(4-Isopropyl-phenoxy)-acetyl]-piperidin-3-yl}-phenoxy)-2-methyl-propionic acid benzyl esterHCID 68885212—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-(3-{1-[(4-Isopropyl-phenoxy)-acetyl]-piperidin-3-yl}-phenoxy)-2-methyl-propionic acidHCID 10433319100%

Reaction Steps

10% Palladium on carbon (4 mg, 10 wt %) was added to a solution of 2-(3-{1-[(4-Isopropyl-phenoxy)-acetyl]-piperidin-3-yl}-phenoxy)-2-methyl-propionic acid benzyl ester (35 mg, 0.066 mmol) in methanol (2 mL) and the resulting mixture hydrogenated at atmospheric pressure for 3 h. The reaction mixture was filtered through a plug of celite and the celite plug washed thoroughly with ethyl acetate. The combined filtrates were concentrated under reduced pressure to provide 29 mg (99%) of 2-(3-{1-[(4-Isopropyl-phenoxy)-acetyl]-piperidin-3-yl}-phenoxy)-2-methyl-propionic acid as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199243B2
Source datasetuspto-grants-2007_04
ORD IDord-ed7e12161e5b4fe8b1d610f56b79f3ca
Source noteuspto-grants-2007_04