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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620578Generated: November 4, 2026

Ammonium Chloride → HCID 86678753, compound

https://huagongshe.com/reaction/1620578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 67504117HCID 67504117—
Reactant1-[2,4-Bis(trifluoromethyl)benzyl]piperidine-4-carbaldehydeHCID 86678663—
SolventEthanolHCID 702—
ProductHCID 86678753HCID 866787530.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-[2,4-bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde (26.0 g) in ethanol (100 mL) were added 4-imino-1-methyl-3-(phenylcarbonyl)imidazolidin-2-one (16.7 g) and potassium tert-butoxide (8.60 g) under ice-cooling. The reaction mixture was stirred at 80° C. for 2 hr. To the reaction mixture was added saturated aqueous ammonium chloride solution at room temperature, and the solvent was evaporated under reduced pressure. Water and ethyl acetate were added to the residue, and the insoluble material was removed by filtration. The filtrate was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate under reduced pressure, and the solvent was evaporated. The residue was purified by silica gel column chromatography (methanol/ethyl acetate) and recrystallized from ethanol/water to give the title compound (270 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-9d774a80f27a479cb1742d59df379b8d
Source noteuspto-grants-2014_07