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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866069Generated: October 30, 2026

Ammonium Chloride → ethyl N-(4-propoxyphenylmethyl)piperidin-4-ylcarboxylate

https://huagongshe.com/reaction/866069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(Chloromethyl)-4-propoxybenzeneHCID 12249108—
SolventDimethyl SulfoxideHCID 679—
Productethyl N-(4-propoxyphenylmethyl)piperidin-4-ylcarboxylateHCID 2200695690.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a stirred solution of 47.5 grams (0.30 mole) of ethyl piperidin-4-ylcarboxylate in 70 mL (0.40 mole) of N,N-diisopropylethylamine was added dropwise a solution of 52.5 grams (0.29 mole) of 4-propoxyphenylmethyl chloride in 50 mL of dimethyl sulfoxide. The reaction caused the reaction mixture temperature to rise to about 35° C. Upon completion of the addition the reaction mixture was stirred for 30 minutes, warmed to 40° C., and then allowed to cool to ambient temperature. After this time the reaction mixture was poured into 500 mL of aqueous 10% ammonium chloride. The mixture was extracted with three 250 mL portions of diethyl ether, and the combined extracts were washed with two 250 mL portions of an aqueous solution saturated with ammonium chloride, one 250 mL portion of water, and one 250 mL portion of an aqueous solution saturated with sodium chloride. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 80.0 grams of ethyl N-(4-propoxyphenylmethyl)piperidin-4-ylcarboxylate. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05569664
Source datasetuspto-grants-1996_10
ORD IDord-05e38349e4f74b1a85de29d92b79a564
Source noteuspto-grants-1996_10