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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233253Generated: October 30, 2026

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

https://huagongshe.com/reaction/2233253

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—
SolventWaterHCID 962—
ProductEthyl 3-methoxy-4-((1-methylpiperidin-4-yl)methoxy)benzoateHCID 21874826111.9%

Reaction Conditions

Temperature95 °C

Reaction Steps

Formaldehyde (35 ml of a 37% solution in water, 420 mmol) was added to a solution of ethyl 3-methoxy-4-(1-tert-butyloxycarbonylpiperidin-4-ylmethoxy)benzoate (35 g, 89 mmol) in formic acid (35 ml) and the reaction was heated at 95° C. for 3 hours. The reaction was cooled, the volatiles we re removed in vacuo and the residue was dissolved in dichloromethane. 3.0N Hydrogen chloride in diethyl ether (40 ml, 120 mmol) was added, together with a little diethyl ether and a solid was precipitated. Collection of the solid by suction filtration followed by drying in vacuo yielded ethyl 3-methoxy-4-(1-methylpiperidin-4-ylmethoxy)benzoate (30.6 g, 100% yield) as a white solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709479B1
Source datasetuspto-grants-2010_05
ORD IDord-5913f3c0222a43d5afb23bb1c9eceaa9
Source noteuspto-grants-2010_05