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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667318Generated: November 4, 2026

Water → HCID 10014061, compound

https://huagongshe.com/reaction/1667318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 67443477HCID 67443477—
SolventDimethylformamideHCID 6228—
SolventMethyl iodideHCID 6328—
SolventTriethylamineHCID 8471—
ProductHCID 10014061HCID 1001406199.2%

Reaction Steps

To a solution of 520 mg of 2-[(E)-2-(2,6-dimethylphenyl)vinyl]piperidine monohydrochloride in 7 ml of dimethylformamide, 0.13 ml of methyl iodide, 0.58 ml of triethylamine and 572 mg of potassium carbonate were added, followed by stirring at ambient temperature for 12 hours. The reaction mixture was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and then dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated and the resulting residue was purified by silica gel column chromatography (chloroform-methanol) to give 470 mg of 2-[(E)-2-(2,6-dimethylphenyl)vinyl]-1-methylpiperidine. The product was dissolved in 5 ml of ethanol, and 2.5 ml of 35% hydrogen chloride-ethanol was added to the solution, followed by stirring at ambient temperature for 1 hour. The reaction mixture was evaporated under reduced pressure and the residue was azeotropically distilled with 5 ml of toluene 3 times to give crystals. The collected crystals were recrystallized from ethanol-ethyl acetate to give 395 mg of 2-[(E)-2-(2,6-dimethylphenyl)vinyl]-1-methylpiperidine monohydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044206B2
Source datasetuspto-grants-2011_10
ORD IDord-68a3badb3c5449b393605417367fa9e6
Source noteuspto-grants-2011_10