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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 237017Generated: October 28, 2026

1-(4-Fluorophenyl)-4-[(4-nitrophenyl)sulfonyl]piperazine → HCID 21314924, compound

https://huagongshe.com/reaction/237017

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Fluorophenyl)-4-[(4-nitrophenyl)sulfonyl]piperazineHCID 1068502—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventChloroformHCID 6212—
ProductHCID 21314924HCID 2131492447.1%

Reaction Steps

A mixture of 5.00 g (0.0137 m) of 1-[(p-nitrophenyl)sulfonyl]-4-(p-fluorophenyl)piperazine, 0.2 g of platinum oxide, and 150 ml of chloroform is shaken under hydrogen on a Parr hydrogenation apparatus for one hour. The mixture is then filtered through a sintered glass funnel containing activated carbon and sand to remove the catalyst. The filtrate is concentrated in vacuo and then extracted with methylene chloride/aqueous sodium bicarbonate. The organic layer is filtered through anhydrous sodium sulfate and taken to dryness. The residue is crystallized from methanol to give 2.16 g of 1-[(p-aminophenyl)sulfonyl]-4-(p-fluorophenyl)piperazine containing a minor impurity. Recrystallization from methanol gives an analytical sample with a melting point of 180.5°-181.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04159331
Source datasetuspto-grants-1979_06
ORD IDord-c0dabf1b92554995b61bf588bccbc459
Source noteuspto-grants-1979_06