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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620486Generated: October 30, 2026

Methyl iodide → HCID 178482467, compound

https://huagongshe.com/reaction/1620486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant1-[2,4-Bis(trifluoromethyl)benzyl]piperidine-4-carbaldehydeHCID 86678663—
ReactantHCID 178482466HCID 178482466—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178482467HCID 17848246716.3%

Reaction Steps

To a solution of 1-[2,4-bis(trifluoromethyl)benzyl]piperidine-4-carbaldehyde (372 mg) in tetrahydrofuran (5 mL) were added potassium tert-butoxide (123 mg) and methyl iodide (0.069 mL) under ice-cooling. The reaction mixture was stirred at room temperature for 1 hr under a nitrogen atmosphere. To the reaction mixture were added saturated aqueous ammonium chloride solution/ethyl acetate, 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) to give an oil. The obtained oil and 4-(methylamino)-1,3-thiazol-2(5H)-one (143 mg) were suspended in ethanol (5 mL), and potassium tert-butoxide (123 mg) was added. The reaction mixture was stirred at 80° C. for 3 hr. To the reaction mixture were added saturated aqueous ammonium chloride solution/ethyl acetate at room temperature, 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 recrystallized from ethyl acetate/heptane to give the title compound (83 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-7f35b5c9b0c54b2d8376297dac5edaba
Source noteuspto-grants-2014_07