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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347878Generated: November 1, 2026

Potassium Iodide → Ethyl 4-(dibenzylamino)-3-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/347878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-amino-3-methoxypiperidine-1-carboxylateHCID 3019430—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-(dibenzylamino)-3-methoxypiperidine-1-carboxylateHCID 19994850—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of racemic ethyl 4-amino-3-methoxypiperidine-1-carboxylate (1 part by mole) in DMF were added benzyl bromide (about 2.2 part by mole), potassium carbonate (about 2.4 part by mole) and potassium iodide (about 0.2 part by mole) respectively. The reaction was heated to about 80° C. After about 6 hours, the reaction was slowly diluted with water (about 12 parts by volume) and extracted with, for example, ethyl acetate. The organic layer was washed with brine and then dried over anhyh. Na2SO4. Subsequent filtration and concentration of the solvent provided the 1 as the yellow-orange oil (1 part by mole).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176218B2
Source datasetuspto-grants-2007_02
ORD IDord-129030bda7da4b999233affec0daf37b
Source noteuspto-grants-2007_02