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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 509267Erstellt: 25. Oktober 2026

Piperazine → 1-(4-(Methylsulfonyl)phenyl)piperazine

https://huagongshe.com/reaction/509267

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperazineHCID 4837—
Edukt1-Bromo-4-(methylsulphonyl)benzeneHCID 77014—
EduktBinap, (A+-)-HCID 634876—
EduktSodium t-butoxideHCID 23676156—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt1-(4-(Methylsulfonyl)phenyl)piperazineHCID 73590420%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

1-Bromo-4-(methylsulfonyl)benzene (275 mg, 1.169 mmol), piperazine (302 mg, 3.507 mmol), Pd2(dba)3 (21 mg, 0.023 mmol), BINAP (44 mg, 0.070 mmol), and sodium-tert-butoxide (169 mg, 1.754 mmol) were suspended in toluene (5 ml), and then the resulting liquid was stirred at 100° C. under nitrogen stream for 15 hours. Distilled water (15 ml) was added to the resulting reaction liquid, followed by extraction with MC (20 ml×3). The organic layer was dried over anhydrous sodium sulfate, followed by filtration and concentration, and then the residue thus obtained was subjected to MPLC (15% MeOH/MC), to obtain 56 mg of pale yellow solid (20%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09096571B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-a98802b486a64799b16b62726b1c72ee
Quellennotizuspto-grants-2015_08