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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497337Generated: October 30, 2026

1-t-butoxycarbonyl-4-[carboxy-(4-fluorophenyl)methyl]-3,6-dihydro-2H-pyridine → 1-t-Butoxycarbonyl-4-[carboxy-(4-fluorophenyl)methyl]piperidine

https://huagongshe.com/reaction/497337

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-t-butoxycarbonyl-4-[carboxy-(4-fluorophenyl)methyl]-3,6-dihydro-2H-pyridineHCID 22318659—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product1-t-Butoxycarbonyl-4-[carboxy-(4-fluorophenyl)methyl]piperidineHCID 2231866771.6%

Reaction Steps

5.0 g of 1-t-Butoxycarbonyl-4-[carboxy-(4-fluorophenyl)methyl]-3,6-dihydro-2H-pyridine was dissolved in 50 ml of methanol, and 0.50 g of palladium hydroxide/carbon was added, followed by stirring under a hydrogen atmosphere at room temperature for 2 days. After removal of the catalyst by Celite filtration, the filtrate was concentrated under reduced pressure to give 3.6 g of a crude 1-t-butoxycarbonyl-4-[carboxy-(4-fluorophenyl)methyl]piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949552B2
Source datasetuspto-grants-2005_09
ORD IDord-490b9368f2424dfbacb0659c2b2eb429
Source noteuspto-grants-2005_09