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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346548Generated: October 27, 2026

Potassium Carbonate → tert-Butyl 4-((4-(ethoxycarbonyl)-2-methoxyphenoxy)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/346548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl vanillateHCID 12038—
Reactant(Piperidin-4-yl)methyl 4-methylbenzene-1-sulfonateHCID 19081872—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-((4-(ethoxycarbonyl)-2-methoxyphenoxy)methyl)piperidine-1-carboxylateHCID 21874806161.7%

Reaction Conditions

Temperature95 °C

Reaction Steps

1-tert-Butoxycarbonyl)-4-(4-methylphenylsulphonyloxymethyl)piperidine (40 g, 0.11 mol), (prepared as described for the starting material in Example 1), was added to a suspension of ethyl 4-hydroxy-3-methoxybenzoate (19.6 g, 0.1 mol) and potassium carbonate (28 g, 0.2 mol) in dry DMF (200 ml). After stirring at 95° C. for 2.5 hours, the mixture was cooled to ambient temperature and partitioned between water and ethyl acetate/ether. The organic layer was washed with water, brine, dried (MgSO4) and evaporated. The resulting oil was crystallised from petroleum ether and the suspension was stored overnight at 5° C. The solid was collected by filtration, washed with petroleum ether and dried under vacuum to give ethyl 4(1-(tert-butoxycarbonyl)piperidin-4-ylmethoxy)-3-methoxybenzoate (35 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173038B1
Source datasetuspto-grants-2007_02
ORD IDord-81e7bd0b28e74333b05ba637db129f38
Source noteuspto-grants-2007_02