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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549945Generated: October 26, 2026

tert-Butyl 4-{4-[(Z)-2-(naphthalen-1-yl)ethenyl]-1,3-thiazol-2-yl}piperidine-1-carboxylate → Tert-butyl 4-{4-[2-(naphthalen-1-yl)ethyl]-1,3-thiazol-2-yl}piperidine-1-carboxylate

https://huagongshe.com/reaction/549945

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-{4-[(Z)-2-(naphthalen-1-yl)ethenyl]-1,3-thiazol-2-yl}piperidine-1-carboxylateHCID 67156180—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl 4-{4-[2-(naphthalen-1-yl)ethyl]-1,3-thiazol-2-yl}piperidine-1-carboxylateHCID 6715668498.2%

Reaction Steps

tert-Butyl 4-{4-[(Z)-2-(naphthalen-1-yl)ethenyl]-1,3-thiazol-2-yl}piperidine-1-carboxylate (IV-3, 1.5 g) is dissolved in 90 ml of methanol and, at 30° C., hydrogenated under a hydrogen pressure of 10 bar using 10% Pd/C as catalyst. Removal of the catalyst by filtration and removal of the solvent under reduced pressure gives tert-butyl 4-{4-[2-(naphthalen-1-yl)ethyl]-1,3-thiazol-2-yl}piperidine-1-carboxylate (1.48 g) as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943774B2
Source datasetuspto-grants-2011_05
ORD IDord-9adc7afb780441da8a430f9dbdc9e3c7
Source noteuspto-grants-2011_05