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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632505Generated: November 3, 2026

Triethylamine → 2-Methoxy-4-[(4-methylpiperazin-1-yl)methyl]benzoic acid methyl ester

https://huagongshe.com/reaction/632505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-MethylpiperazineHCID 53167—
ReactantMethyl 4-(bromomethyl)-2-methoxybenzoateHCID 11288398—
SolventEthanolHCID 702—
Product2-Methoxy-4-[(4-methylpiperazin-1-yl)methyl]benzoic acid methyl esterHCID 11788892485%

Reaction Steps

To 100 mL of ethanol were added 10.0 g of 1-methylpiperazine and 20.2 g of triethylamine. To the mixture cooled with ice, 25 mL of a solution of 24.6 g of 4-(bromomethyl)-2-methoxy-benzoic acid methyl ester in ethanol was added dropwise. The mixture was stirred at room temperature for 18 hours. The reaction mixture was concentrated. To the residue, 75 mL of water and 250 mL of methylene chloride were added, and the organic layer was separated. The obtained organic layer was dried over Na2SO4 and concentrated. The residue was purified by amino-silica gel column chromatography (heptane/AcOEt system) to give 22.4 g of the title compound (85% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321752B2
Source datasetuspto-grants-2016_04
ORD IDord-ee31b6255db64fbd9a3ebe8ab054d666
Source noteuspto-grants-2016_04