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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477041Generated: October 30, 2026

Piperazine → HCID 14903418, compound

https://huagongshe.com/reaction/477041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium CarbonateHCID 11430—
ReactantBromodiphenylmethaneHCID 236603—
ReactantHCID 14903424HCID 14903424—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 14903418HCID 1490341857%

Reaction Steps

The product of (1) (the piperazine compound) (5.996 g, 29.1 mmol) was put in a 100 ml-three-necked flask, which was equipped with a Dimroth condenser on the central mouth and septum rubbers on the side mouths. In the flask, DMF (33 ml) was added to dissolve the content, and potassium carbonate (8.034 g, 58.1 mmol) and bromodiphenylmethane (7.543 g, 30.5 mmol) were added. The mixture was stirred at room temperature for 2 hours. The reaction mixture was added to water (80 ml) in a 200 ml-conical flask, and the mixture was extracted with diethyl ether (four times, 100 ml each time). The ether layer was washed with brine (twice, 40 ml each time), dried and distilled off under reduced pressure. The residue (10.616 g) was subjected to column chromatography [silica gel, ethyl acetate-n-hexane (1:1)] for separation and purification to give 6.188 g of the above-captioned benzhydrylpiperazine compound (Yield: 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886819
Source datasetuspto-grants-1989_12
ORD IDord-80f15a1081a34e309579f0e9956d199e
Source noteuspto-grants-1989_12