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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013390Generated: October 31, 2026

1-Benzyl-5-thiophen-3-yl-1,2,3,6-tetrahydro-pyridine-4-carboxylic acid ethyl ester → 1-Benzyl-3-thiophen-3-yl-piperidine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1013390

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-5-thiophen-3-yl-1,2,3,6-tetrahydro-pyridine-4-carboxylic acid ethyl esterHCID 59789438—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1-Benzyl-3-thiophen-3-yl-piperidine-4-carboxylic acid ethyl esterHCID 6720672271%

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of the product from step b) (6.69 g, 20.4 mmol) was dissolved in EtOH (37 ml) and treated with 10% Pd/C (Wet Degussa type, 13.4 g) and heated to 40° C. for 2 days under H2 (1 atm). Next, the Pd/C was removed by filtration through celite, replaced with fresh 10% Pd/C (13.4 g) and the reaction was continued for two more days. The Pd/C was removed by filtration through celite and the EtOH was evaporated in vacuo to provide the subtitle compound (4.78 g, 71%). MS calculated for C19H23NO2S+H 330, observed 330.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981919B2
Source datasetuspto-grants-2011_07
ORD IDord-2c943251d49543b8b798ff39b3f7e9c0
Source noteuspto-grants-2011_07