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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620467Generated: November 1, 2026

tert-Butyl 4-formylpiperidine-1-carboxylate → HCID 178482474, compound

https://huagongshe.com/reaction/1620467

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178482466HCID 178482466—
SolventEthanolHCID 702—
ProductHCID 178482474HCID 17848247451.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

tert-Butyl 4-formylpiperidine-1-carboxylate (1.61 g) and 4-(methylamino)-1,3-thiazol-2(5H)-one (1.18 g) were suspended in ethanol (10 mL), potassium tert-butoxide (1.02 g) was added, and the mixture was stirred at 80° C. for 8 hr. The reaction mixture was concentrated, saturated aqueous ammonium chloride solution was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with 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 (NH, ethyl acetate/hexane) to give the title compound (1.27 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-a2ab593111f2466c8984bed50b0ee5f8
Source noteuspto-grants-2014_07