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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334433Generated: October 25, 2026

Trichloroacetic Acid → 2,2,2-Trichloro-1-(4-(4-methylpiperazine-1-yl)phenyl)ethanol

https://huagongshe.com/reaction/334433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetic AcidHCID 6421—
Reactant4-(4-Methylpiperazin-1-yl)benzaldehydeHCID 736533—
ReactantSodium TrichloroacetateHCID 23681045—
SolventDimethylformamideHCID 6228—
Product2,2,2-Trichloro-1-(4-(4-methylpiperazine-1-yl)phenyl)ethanolHCID 6827717282%

Reaction Steps

1.0 ml (10.00 mmol) of trichloroacetic acid and, in small portions, 1.854 g. (10 mmol) of sodium 2,2,2-trichloroacetate are added at room temperature to a solution of 1.362 g (6.67 mmol) of 4-(4-methylpiperazine-1-yl)benzaldehyde in 13.5 ml of dimethylformamide. The reaction mixture is stirred for 3 hours at room temperature. The solvent is concentrated and the crude reaction product extracted with ethyl acetate. The organic phase is washed using saturated sodium bicarbonate solution. The organic phases are combined, dried on magnesium sulfate and then concentrated to yield 1.760 g (yield=82%) of 2,2,2-trichloro-1-(4-(4-methylpiperazine-1-yl)phenyl)ethanol in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883821B2
Source datasetuspto-grants-2014_11
ORD IDord-515ca87369a043708f8648e14abc16e2
Source noteuspto-grants-2014_11