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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416668Generated: October 31, 2026

Water → 1-[5-(4-Methoxy-benzenesulfonyl)2-methoxy-phenyl]piperazine

https://huagongshe.com/reaction/2416668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant4-Methoxy-3-[4-(2,2,2-trifluoro-acetyl)-piperazin-1-yl]-benzenesulfonyl chlorideHCID 12136655—
ReactantHCID 178491912HCID 178491912—
SolventTetrahydrofuranHCID 8028—
Product1-[5-(4-Methoxy-benzenesulfonyl)2-methoxy-phenyl]piperazineHCID 996896036%

Reaction Steps

To a solution of 4-methoxy-3-[4-(2,2,2-trifluoro-acetyl)-piperazin-1-yl]-benzenesulfonyl chloride (0.19 g), prepared as in Example 1 Step 2, in THF (0.5 ml) at 0° C. under argon atmosphere was added dropwise a solution of 4-methoxyphenylmagnesium bromide in THF (0.5M, 2 ml; 1 mmol). After stirring at this temperature for 1 h. A solution of 6N NaOH (0.5 ml) was added and the reaction mixture was stirred at ambient temperature for 20 h. Water was added (10 ml) and the mixture was extracted into ethyl acetate (20 ml). The organic phase was dried (Na2SO4) and concentrated in vacuo to give 1-[5-(4-methoxy-benzenesulfonyl)2-methoxy-phenyl]piperazine as a white solid (0.65 g, 36%), MS, MH+ 363.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825202B2
Source datasetuspto-grants-2004_11
ORD IDord-749f4815bc714a1d877f34835426b867
Source noteuspto-grants-2004_11