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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048799Generated: October 26, 2026

Ethanol → [4-(4-Methyl-piperazin-1-yl)-phenyl]-acetic acid

https://huagongshe.com/reaction/1048799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantDibenzyl diselenideHCID 95955—
ReactantSodium borohydrideHCID 4311764—
Reactant2,2,2-Trichloro-1-(4-(4-methylpiperazine-1-yl)phenyl)ethanolHCID 68277172—
Product[4-(4-Methyl-piperazin-1-yl)-phenyl]-acetic acidHCID 28807075—

Reaction Steps

0.559 g (14.77 mmol) of sodium borohydride is added quickly to 2.294 g (7.35 mmol) of dibenzyl diselenide in 28 ml of ethanol. The reaction mixture is stirred at room temperature for 1 hour. 2.266 g (7 mmol) of 2,2,2-trichloro-1-(4-(4-methylpiperazine-1-yl)phenyl)ethanol and 1.680 g (42.0 mmol) of sodium hydroxide are then added. The reaction mixture is stirred at 35° C. for 24 hours. The solvent is concentrated and the crude product extracted with ethyl acetate after adding a pH 5 aqueous phase. The organic phases are combined, dried on magnesium sulfate and then concentrated to yield 2-(4-(4-methylpiperazine-1-yl)phenyl)acetic acid which is used without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09381195B2
Source datasetuspto-grants-2016_07
ORD IDord-1cf5ad2b3e3f4b46a07e3d3f89283128
Source noteuspto-grants-2016_07