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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534822Generated: October 31, 2026

Hydrochloric Acid → Piperazine, 1-[4-bromo-2-(1,1-dimethylethyl)phenyl]-, hydrochloride (1:2)

https://huagongshe.com/reaction/534822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantBis(2-chloroethyl)amine hydrochlorideHCID 522769—
Reactant4-bromo-2-tert-butylphenylamineHCID 11959000—
SolventDiethyl EtherHCID 3283—
SolventDiglymeHCID 8150—
SolventEthyl AcetateHCID 8857—
ProductPiperazine, 1-[4-bromo-2-(1,1-dimethylethyl)phenyl]-, hydrochloride (1:2)HCID 6675114240%

Reaction Conditions

Temperature170 °C

Reaction Steps

A suspension of 4-bromo-2-tert-butylaniline (Reference Example 8, 25.0 g, 110 mmol) and bis(2-chloroethyl)amine hydrochloride (21.5 g, 120 mmol) in diethylene glycol dimethyl ether (157 mL) was stirred for 3 days at 170° C. It was cooled to room temperature, added 1 M sodium hydroxide solution (50 mL), and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give crude product. It was diluted with ethyl acetate and ether (50:50) and added 1 M hydrochloric acid solution to provide 1-(4-bromo-2-tert-butylphenyl)piperazine dihydrochloride (16.2 g, 40%) as a gray solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-aded8697d3b843e78c6180e5a9014580
Source noteuspto-grants-2014_10