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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643562Generated: November 1, 2026

tert-butyl 4-(3-cyanophenyl)-3,6-dihydropyridine-1(2H)-carboxylate → Tert-butyl 4-(3-cyanophenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/643562

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-(3-cyanophenyl)-3,6-dihydropyridine-1(2H)-carboxylateHCID 51356836—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductTert-butyl 4-(3-cyanophenyl)piperidine-1-carboxylateHCID 59261051—

Reaction Steps

tert-Butyl 4-(3-cyanophenyl)-3,6-dihydropyridine-1(2H)-carboxylate (1.00 g, 3.52 mmol) was combined with 20% Pd(OH)2/C (1 g) in 25 mL of methanol. This mixture was stirred under a hydrogen atmosphere using a hydrogen filled balloon for 5 h. The reaction mixture was filtered through a celite plug and the filtrate was concentrated. Purification by MPLC (silica, 38% ethyl acetate/hexanes) gave tert-butyl 4-(3-cyanophenyl)piperidine-1-carboxylate. ESI-MS calc. for C17H22N2O2: 286; Found: 309 (M+Na+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700591B2
Source datasetuspto-grants-2010_04
ORD IDord-65dd06ae8dbd43c386a29133bc3d4910
Source noteuspto-grants-2010_04