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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373588Generated: October 30, 2026

1-(3-Chlorophenyl)piperazine → HCID 19810680, compound

https://huagongshe.com/reaction/373588

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Chlorophenyl)piperazineHCID 1355—
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-N-trityl-1-propanamineHCID 256581—
SolventWaterHCID 962—
ProductHCID 19810680HCID 19810680105.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 5.9 g (30 mmol) of 1-(3-chlorophenyl)piperazine, 12.55 g (33 mmol) of 3-bromo-N-(triphenylmethyl)propanamine, 6.2 g (45 mmol) of potassium carbonate and 60 ml of dimethylformamide is stirred at 90° C. for 6.5 h under argon. The mixture is then poured into iced water and is extracted with ethyl acetate. The organic phase is separated off, is washed with water, is dried and the solvent is evaporated off. 15.7 g of oily residue are obtained and are purified by chromatography on a column of silica gel by eluting with a 99/1 dichloromethane/methanol mixture, which yields 11.8 g of light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05164397
Source datasetuspto-grants-1992_11
ORD IDord-e3c920a3bcb142418c69e20935593b80
Source noteuspto-grants-1992_11