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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620586Generated: November 1, 2026

Ammonium Chloride → HCID 178482463, compound

https://huagongshe.com/reaction/1620586

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 178482463HCID 1784824630.6%

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 ethanol was evaporated under reduced pressure. Water and ethyl acetate were added to the residue, and the insoluble material was collected by filtration. The obtained solid was recrystallized from water/ethanol and further recrystallized from water/acetone for purification. To a solution of the obtained solid (2.03 g) in toluene (10 mL) was added a solution (4.8 mL) of methylamine in 40% methanol at room temperature. The reaction mixture was stirred at 70° C. overnight, a solution (4.8 mL) of methylamine in 40% methanol was added at room temperature, and the mixture was stirred at 70° C. overnight. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (NH, methanol/ethyl acetate) and recrystallized from heptane to give the title compound (223 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-5b27fa36c8ab4398ae323c65dcead25c
Source noteuspto-grants-2014_07