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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482484Generated: October 26, 2026

Hydrogen Bromide → 1-(2-Phenoxy-2-methylpropionyl)piperazine hydrochloride

https://huagongshe.com/reaction/482484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantPiperazineHCID 4837—
Reactant2-Methyl-2-phenoxypropanoyl chlorideHCID 13111191—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Phenoxy-2-methylpropionyl)piperazine hydrochlorideHCID 19063091—

Reaction Steps

To a solution of 17.2 g of anhydrous piperazine in 50 ml of EtOH 95% and 22 ml of H2O, 3.37 g of HBr 48% are dropped in about 10' and thereafter, in about 40' and at room temperature, a solution of 9.93 g of 2-phenoxy-2-methylpropionyl chloride (prepared according to: Bull. Soc. Chim. Fr. 1956, 776-783) in 70 ml of THF. The suspension is stirred 2 h at the same temperature and 3 h under reflux, diluted with 130 ml of THF, cooled, and the piperazine salts precipitated are filtered away. The filtered is evaporated to dryness, the residue is resuspended with 120 ml of H2O and 35 ml HCl 2N and extracted with Et2O; the aqueous phase is treated with 40 ml NaOH conc. and extracted with Et2O (4×50 ml). The ethere-phase, dried, is treated with HCl in Et2 O about 3N and the precipitate is collected by filtration and crystallized from EtOH giving 5.98 g (42%) of the wanted compound; m.p.: 236°-238° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05798362
Source datasetuspto-grants-1998_08
ORD IDord-9c5d21b2958d4cd99eb87f76a021a55d
Source noteuspto-grants-1998_08