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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620478Generated: October 27, 2026

Potassium tert-butoxide → HCID 178456914, compound

https://huagongshe.com/reaction/1620478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactant1-[2,4-Bis(trifluoromethyl)benzyl]piperidine-4-carbaldehydeHCID 86678663—
ReactantHCID 178456890HCID 178456890—
SolventEthanolHCID 702—
ProductHCID 178456914HCID 17845691447.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 1-[2,4-bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde (15 g) and 4-(prop-2-yn-1-ylamino)-1,3-thiazol-2(5H)-one (8.18 g) in ethanol (150 mL) was added potassium tert-butoxide (5.95 g), and the reaction mixture was stirred at 80° C. for 30 min. The reaction mixture was concentrated, saturated aqueous ammonium chloride solution/ethyl acetate were added to the residue, and the organic layer was separated, 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 the residue was washed with diisopropyl ether to give the title compound (9.96 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-8dfc4a285f7d4befbd764aec0438a911
Source noteuspto-grants-2014_07