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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577363Generated: October 29, 2026

Hydrochloric Acid → Ethyl 3-methoxy-4-((1-methylpiperidin-4-yl)methoxy)benzoate

https://huagongshe.com/reaction/577363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantDiethyl EtherHCID 3283—
Reactanttert-Butyl 4-((4-(ethoxycarbonyl)-2-methoxyphenoxy)methyl)piperidine-1-carboxylateHCID 21874806—
SolventFormic AcidHCID 284—
ProductEthyl 3-methoxy-4-((1-methylpiperidin-4-yl)methoxy)benzoateHCID 21874826111.9%

Reaction Conditions

Temperature95 °C

Reaction Steps

Formaldehyde (12M, 37% in water, 35 ml, 420 mmol) was added to a solution of ethyl 4-(1-(tert-butoxycarbonyl)piperidin-4-ylmethoxy)-3-methoxybenzoate (35 g, 89 mmol) in formic acid (35 ml). After stirring at 95° C. for 3 hours, the volatiles were removed by evaporation. The residue was dissolved in methylene chloride and 3M hydrogen chloride in ether (40 ml, 120 mmol) was added. After dilution with ether, the mixture was triturated until a solid was formed. The solid was collected by filtration, washed with ether and dried under vacuum overnight at 50° C. to give ethyl 3-methoxy-4-(1-methylpiperidin-4-ylmethoxy)benzoate (30.6 g, quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040548B2
Source datasetuspto-grants-2015_05
ORD IDord-aba819ddf5284663825db648ccbe67be
Source noteuspto-grants-2015_05