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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295487Generated: October 30, 2026

1-Phenylpiperazine → HCID 70504599, compound

https://huagongshe.com/reaction/2295487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantTriethylamineHCID 8471—
ReactantBenzenesulfinyl chlorideHCID 4190003—
SolventDichloromethaneHCID 6344—
ProductHCID 70504599HCID 70504599—

Reaction Steps

To a solution of 4.87 g of N-phenylpiperazine in 150 ml of dichloromethane containing 4.59 ml of triethylamine is added dropwise with stirring under nitrogen a solution of 4.82 g of benzenesulfinyl chloride in 50 ml of dichloromethane. The reaction mixture is stirred for 3 hours at room temperature, diluted with 100 ml of dichloromethane and washed with 150 ml of water and 100 ml of 5% potassium carbonate solution. The organic layer is dried over anhydrous sodium sulfate and evaporated in vacuo to a nearly colorless crystalline solid. Recrystallization from ethanol affords 6.37 g of 1-phenylpiperazine-4-benzenesulfinamide as a nearly colorless crystalline solid, mp, 101°-104° (softens 98°).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04425342
Source datasetuspto-grants-1984_01
ORD IDord-24acb2bef74e4a7da78631e1b19d002d
Source noteuspto-grants-1984_01