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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816969Generated: November 1, 2026

tert-butyl 4-[3-(ethoxycarbonyl)phenyl]-3,6-dihydropyridine-1(2H)-carboxylate → Tert-butyl 4-[3-(ethoxycarbonyl)phenyl]piperidine-1-carboxylate

https://huagongshe.com/reaction/1816969

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-[3-(ethoxycarbonyl)phenyl]-3,6-dihydropyridine-1(2H)-carboxylateHCID 57880536—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductTert-butyl 4-[3-(ethoxycarbonyl)phenyl]piperidine-1-carboxylateHCID 57880576—

Reaction Steps

A mixture of tert-butyl 4-[3-(ethoxycarbonyl)phenyl]-3,6-dihydropyridine-1(2H)-carboxylate (6.48 g, 19.6 mmol) and Pd(OH)2/C (20% Pd, 1 g) in 50 mL of methanol was stirred under a hydrogen atmosphere (balloon) for 18 h. The reaction mixture was then filtered through a celite plug, and the filtrate was concentrated to give tert-butyl 4-[3-(ethoxycarbonyl)phenyl]piperidine-1-carboxylate which did not require further purification. 1HNMR (CDCl3, 500 MHz): δ 7.91 (m, 2H), 7.40 (m, 2H), 4.40 (q, J=7.0 Hz, 2H), 4.28 (br s, 2H), 2.83 (m, 2H), 2.73 (tt, J=12.5, 4.0 Hz, 1H), 1.85 (br d, J=13.0 Hz), 1.67 (dq, J=4.0, 12.5 Hz, 2H), 1.51 (s, 9H), 1.42 (t, J=7.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598243B2
Source datasetuspto-grants-2009_10
ORD IDord-486c0bf792614ee798d6aadcc2432dc0
Source noteuspto-grants-2009_10