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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767729Generated: October 31, 2026

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

https://huagongshe.com/reaction/1767729

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 removed in vacuo and the residue was dissolved in dichloromethane. 3.0 N 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 numberUS07235559B1
Source datasetuspto-grants-2007_06
ORD IDord-b51fef20406d493abec03084bf35be17
Source noteuspto-grants-2007_06