HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 509267Erstellt: 25. Oktober 2026
Piperazine → 1-(4-(Methylsulfonyl)phenyl)piperazine
https://huagongshe.com/reaction/509267
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Piperazine | HCID 4837 | — |
| Edukt | 1-Bromo-4-(methylsulphonyl)benzene | HCID 77014 | — |
| Edukt | Binap, (A+-)- | HCID 634876 | — |
| Edukt | Sodium t-butoxide | HCID 23676156 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1-(4-(Methylsulfonyl)phenyl)piperazine | HCID 735904 | 20% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09096571B2 |
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| Quelldatensatz | uspto-grants-2015_08 |
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| ORD ID | ord-a98802b486a64799b16b62726b1c72ee |
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| Quellennotiz | uspto-grants-2015_08 |
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