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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095003Generated: October 31, 2026

Piperidine → Ethyl 3,4-bis(2-methoxyethoxy)benzoate

https://huagongshe.com/reaction/1095003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3,4-DihydroxybenzoateHCID 77547—
Reactant2-Amino-5-piperidin-1-yl-benzoic acid ethyl esterHCID 61306567—
SolventAcetoneHCID 180—
ProductEthyl 3,4-bis(2-methoxyethoxy)benzoateHCID 280899293%

Reaction Conditions

Temperature70 °C

Reaction Steps

3,4-Dihydroxy-benzoic acid ethyl ester (compound A′) (2.0 g) was dissolved in acetone (20 ml). Potassium carbonate (4.3 g) and 1-bromo-2-methoxy-ethane (compound D) (5 ml) were added to the solution at room temperature, and the mixture was then stirred at 70° C. for 24 hr. After the completion of the reaction, the reaction solution was allowed to stand for cooling at room temperature, and the reaction system was concentrated under the reduced pressure. Distilled water was added to the residue, and the mixture was then subjected to separatory extraction with chloroform. The organic layer was washed with saturated brine, was dried over sodium sulfate, and was then concentrated under the reduced pressure. The residue was purified by column chromatography using a hexane-acetone system to give 3,4-bis-(2-methoxy-ethoxy)-benzoic acid ethyl ester (3.06 g, yield 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134015B2
Source datasetuspto-grants-2012_03
ORD IDord-c7a9a14c1a3f443d9414d55c47afcadd
Source noteuspto-grants-2012_03