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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800427Generated: October 26, 2026

Trifluoroacetic acid → 2-(4-Methylpiperazin-1-yl)acetic acid dihydrochloride

https://huagongshe.com/reaction/1800427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 2-(4-methylpiperazin-1-yl)acetateHCID 11816730—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
Product2-(4-Methylpiperazin-1-yl)acetic acid dihydrochlorideHCID 4489142488%

Reaction Steps

tert-Butyl(4-methylpiperazin-1-yl)acetate (3.50 g, 16.3 mmol) was suspended in 4N hydrogen chloride/1,4-dioxane (35 mL) solution, trifluoroacetic acid (60 mL) was added to give a solution, and the solution was stirred at room temperature for 4 hr. The reaction mixture was concentrated under reduced pressure, 4N hydrogen chloride/ethyl acetate (30 mL) was added to the obtained oily residue to give a suspension, and the suspension was stirred at room temperature for 2 hr. The obtained precipitate was collected by filtration, washed with ethyl acetate and diisopropyl ether on filter paper, and dried to give the title compound (3.33 g, 88%) as a colorless powder. The compound was used for the next reaction without further purification operation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344135B2
Source datasetuspto-grants-2013_01
ORD IDord-c73d1d5999af4b3ab1ab730e67563879
Source noteuspto-grants-2013_01