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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl 2-(4-methylpiperazin-1-yl)acetate | HCID 11816730 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Product | 2-(4-Methylpiperazin-1-yl)acetic acid dihydrochloride | HCID 44891424 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344135B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-c73d1d5999af4b3ab1ab730e67563879 |
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| Source note | uspto-grants-2013_01 |
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