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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670747Generated: October 29, 2026

tert-Butyl piperazine-1-carboxylate → HCID 23149920, compound

https://huagongshe.com/reaction/1670747

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant5-Bromo-2-fluorobenzotrifluorideHCID 2736325—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ReactantHCID 86613788HCID 86613788—
SolventEthyl AcetateHCID 8857—
ProductHCID 23149920HCID 2314992075%

Reaction Steps

By a similar operation as in Starting Material Synthetic Example 16, 4-[4-fluoro-3-(trifluoromethyl)phenyl]piperazine-1-carboxylic acid tert-butyl ester was synthesized from 5-bromo-2-fluorobenzotrifluoride (Aldrich Co., 1.5 g) and 1-(tert-butoxycarbonyl)piperazine (1.38 g). These were dissolved in ethyl acetate, 4N hydrochloric acid-ethyl acetate was added, and the mixture was stirred at room temperature for 6 hr. The precipitated solid was collected by filtration and dried to give 1-[4-fluoro-3-(trifluoromethyl)phenyl]piperazine hydrochloride (1.31 g, yield 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994196B2
Source datasetuspto-grants-2011_08
ORD IDord-1fdeca183588442783c126ab47726f5c
Source noteuspto-grants-2011_08