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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620473Generated: November 3, 2026

tert-Butyl 4-formylpiperidine-1-carboxylate → HCID 86678665, compound

https://huagongshe.com/reaction/1620473

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
Reactant4-Sulfanylidene-1,3-thiazolidin-2-oneHCID 1539595—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86628739HCID 86628739—
SolventEthanolHCID 702—
ProductHCID 86678665HCID 8667866566.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

tert-Butyl 4-formylpiperidine-1-carboxylate (7.6 g) and 4-thioxo-1,3-thiazolidin-2-one (4.98 g) were suspended in ethanol (200 mL), potassium tert-butoxide (4.80 g) was added, and the reaction mixture was stirred at 80° C. for 4 hr. Acetic acid/water/ethyl acetate were added to the reaction mixture, and the organic layer was separated, washed with saturated aqueous sodium hydrogen carbonate solution 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 washed with diethyl ether to give the title compound (7.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-9690bea49a354c56b701fe801f265ef5
Source noteuspto-grants-2014_07