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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620539Generated: October 29, 2026

tert-Butyl 4-formylpiperidine-1-carboxylate → HCID 178459309, compound

https://huagongshe.com/reaction/1620539

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantPiperidinium acetateHCID 3014295—
ReactantHCID 178459301HCID 178459301—
SolventIsopropanolHCID 3776—
ProductHCID 178459309HCID 17845930956.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of tert-butyl 4-formylpiperidine-1-carboxylate (1.70 g) in 2-propanol (30 mL) were added 4-[(2-hydroxy-2-methylpropyl)amino]-1,3-thiazol-2(5H)-one (3.00 g), and piperidinium acetate (1.18 g). The reaction mixture was stirred at 60° C. overnight and concentrated. Water was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) and recrystallized from ethyl acetate/heptane to give the title compound (1.72 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-ee73697c73c648b79eb019390daf09cb
Source noteuspto-grants-2014_07