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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419569Generated: November 3, 2026

t-Butyl (1-t-Butoxycarbonyl-1,2,3,6-tetrahydropyridin-4-yl)phenylcarbamate → t-Butyl (1-t-Butoxycarbonylpiperidin-4-yl)phenylcarbamate

https://huagongshe.com/reaction/1419569

Reaction equation

Participants

RoleNameHCIDCharge
Reactantt-Butyl (1-t-Butoxycarbonyl-1,2,3,6-tetrahydropyridin-4-yl)phenylcarbamateHCID 53951936—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Productt-Butyl (1-t-Butoxycarbonylpiperidin-4-yl)phenylcarbamateHCID 5439208697.1%

Reaction Steps

t-Butyl (1-t-butoxycarbonyl-1,2,3,6-tetrahydropyridin-4-yl)phenylcarbamate (2.5 g) was dissolved in ethanol, palladium on carbon (10%) was added and the mixture was shaken under hydrogen (50 psi.) for 3 h. The mixture was filtered through Hyflo and the solvent was evaporated under reduced pressure. The residue was purified by MPLC on silica gel, eluting with EtOAc/Hexane (5:95) to give the title compound as a clear oil (2.44 g), δH (CDCl3) 1.51 (9H, s), 1.55 (9H, s), 1.69 (2H, m), 1.79 (2H, m), 2.77 (3H, m), 4.24 (2H, m), 6.18 (1H, br s), 7.12-7.18 (3H, m), 7.52 (1H, m). m/e (CI+) 377 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885999
Source datasetuspto-grants-1999_03
ORD IDord-557fc6d3aded4f40ad1e18d62f58044e
Source noteuspto-grants-1999_03