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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634852Generated: October 30, 2026

Potassium Carbonate → ethyl N-[2-(4-methoxyphenyl)ethyl]piperidin-4-ylcarboxylate

https://huagongshe.com/reaction/634852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
Reactant4-(2-Chloroethyl)phenyl methyl etherHCID 87513—
SolventDimethylformamideHCID 6228—
Productethyl N-[2-(4-methoxyphenyl)ethyl]piperidin-4-ylcarboxylateHCID 1539016525.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

A stirred mixture of 5.0 grams (0.032 mole) of ethyl piperidin-4-ylcarboxylate, 5.4 grams (0.032 mole) of 1-(2-chloroethyl)-4-methoxybenzene and 4.4 grams (0.032 mole) of potassium carbonate in 50 mL of dried N,N-dimethylformamide was heated at 70° C. for about 16 hours. After this time the reaction mixture was cooled and partitioned between diethyl ether and water. The organic layer was separated and washed with water and then with an aqueous solution saturated with sodium chloride. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residue, which was subjected to column chromatography on silica gel, with diethyl ether/hexane mixtures as eluants. The product-containing fractions were combined and concentrated under reduced pressure, yielding 2.4 grams of ethyl N-[2-(4-methoxyphenyl)ethyl]piperidin-4-ylcarboxylate. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184234B2
Source datasetuspto-grants-2001_02
ORD IDord-a1857def8c404b4fb011bc0ac486b66b
Source noteuspto-grants-2001_02