HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 41292Erstellt: 26. Oktober 2026
Sodium Hydroxide → (S)-3-Methyl-1-((4-(trifluoromethyl)phenyl)sulfonyl)piperazine
https://huagongshe.com/reaction/41292
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2-Methylpiperazine, (S)- | HCID 2734219 | — |
| Edukt | 4-(Trifluoromethyl)benzenesulfonyl chloride | HCID 2777399 | — |
| Katalysator | 4-(Trifluoromethyl)benzenesulfonyl chloride | HCID 2777399 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (S)-3-Methyl-1-((4-(trifluoromethyl)phenyl)sulfonyl)piperazine | HCID 59152086 | 64,9% |
Reaktionsschritte
(2S)-2-methylpiperazine (15 g, 150 mmol) was dissolved in tetrahydrofuran (300 mL) and the solution was cooled down to 0° C. Sodium hydroxide (150 mL, 449 mmol) was added, then 4-(trifluoromethyl)benzenesulfonyl chloride (40 g, 164 mmol) (dissolved in 200 ml THF) was added dropwise and the resulting mixture was stirred for 1 h. Further 4-(trifluoromethyl)benzenesulfonyl chloride (0.06 eq, 2.2 g) was added and mixture stirred for 10 min. The mixture was diluted with DCM (500 ml) and water (500 ml) and stirred for 5 min. The phases were separated, the aqueous layer was extracted with DCM (1000 ml) and the organic phases concentrated under reduced pressure. The residue was taken-up with 1 M HCl (500 ml) and washed with DCM in order to extracted impurities. The aqueous phase was basified to pH=9 with NaOH 3M, extracted with DCM (3×500 ml) and the combined organic phases dried over Na2SO4 before the solvent was removed under reduced pressure to give the title compound (30 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08530478B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-f742b54143bd46a885d553ad56c792e3 |
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| Quellennotiz | uspto-grants-2013_09 |
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