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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269507Generated: November 1, 2026

3-[3-(1-Benzyloxycarbonyl-1-methyl-ethoxy)-phenyl]-piperidine-1-carboxylic acid 4-isopropyl-phenyl ester → 3-[3-(1-Carboxy-1-methyl-ethoxy)-phenyl]-piperidine-1-carboxylic acid 4-isopropyl-phenyl ester

https://huagongshe.com/reaction/1269507

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[3-(1-Benzyloxycarbonyl-1-methyl-ethoxy)-phenyl]-piperidine-1-carboxylic acid 4-isopropyl-phenyl esterHCID 68882937—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-[3-(1-Carboxy-1-methyl-ethoxy)-phenyl]-piperidine-1-carboxylic acid 4-isopropyl-phenyl esterHCID 9845323—

Reaction Steps

10% Palladium on carbon (180 mg, 10 wt %) was added to a solution of 3-[3-(1-Benzyloxycarbonyl-1-methyl-ethoxy)-phenyl]-piperidine-1-carboxylic acid 4-isopropyl-phenyl ester (1.76 g, 3.41 mmol) in methanol (15 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 1.26 g (87%) of: 3-[3-(1-Carboxy-1-methyl-ethoxy)-phenyl]-piperidine-1-carboxylic acid 4-isopropyl-phenyl ester as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199243B2
Source datasetuspto-grants-2007_04
ORD IDord-9401ba8d903d42fc92b85fdcbed4ee5f
Source noteuspto-grants-2007_04