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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974628Generated: October 29, 2026

1-Phenylpiperazine → HCID 15053393, compound

https://huagongshe.com/reaction/974628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantHCID 15053366HCID 15053366—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15053393HCID 1505339348.1%

Reaction Steps

A solution of 2.9 g (0.01 mole) of 3-(4-bromophenoxy)-1-azetidinecarbonyl chloride in 15 ml of tetrahydrofuran was treated while stirring with 1.6 g (0.01 mole) of 1-phenylpiperazine added all at once, a solid formed instantaneously and after stirring for 2 hr, the reaction mixture was diluted with 200 ml of water, the solid did not dissolve. The solid was removed by filtration and when triturated with chloroform, all but about 1 g of solid dissolved. The chloroform solution was dried over magnesium sulfate then concentrated in vacuo. The oily residue crystallized when triturated with ligroin. Recrystallization from benzene/ligroin yielded 2.0 g (48.1%) of fine white crystals, m.p. 160°-161° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05068231
Source datasetuspto-grants-1991_11
ORD IDord-3b9dbcaa54a44e49940a330acc9d09d9
Source noteuspto-grants-1991_11