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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929759Generated: November 1, 2026

Water → HCID 68916809, compound

https://huagongshe.com/reaction/1929759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantBenzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
ProductHCID 68916809HCID 6891680921%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of benzyl 4-hydroxy-1-piperidinecarboxylate (1.0 g) in toluene/aqueous 2N sodium hydroxide solution (10 mL/10 mL) was added tetrabutylammonium bromide (550 mg) and methoxyethyl bromide (1.2 mL) and the mixture was stirred at 60° C. for 2.5 hours and then stirred at 80° C. for 17 hours. To the reaction mixture was added sodium hydroxide (0.95 g) and methoxyethyl bromide (1.2 mL) and the mixture was stirred at 80° C. for 24 hours. After cooling to room temperature, to the reaction mixture was added water and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated brine, dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo and the resultant crude product was purified by column chromatography on silica gel (solvent; hexane/ethyl acetate=75/25 to 40/60) to give benzyl 4-(2-methoxyethoxy)-1-piperidinecarboxylate (266 mg, yield: 21%) as a pale yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188097B2
Source datasetuspto-grants-2012_05
ORD IDord-366cdb6245f949c8b9a07012244ac215
Source noteuspto-grants-2012_05