HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1868126Erstellt: 26. Oktober 2026
Toluene → (R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazine
https://huagongshe.com/reaction/1868126
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Toluene | HCID 1140 | — |
| Edukt | alpha,alpha,alpha,3-Tetrafluorotoluene | HCID 67867 | — |
| Edukt | 2-Methylpiperazine, (R)- | HCID 7330434 | — |
| Edukt | Sodium t-butoxide | HCID 23676156 | — |
| Katalysator | Binap, (A+-)- | HCID 634876 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazine | HCID 68554948 | 33,6% |
Reaktionsschritte
(R)-2-methyl-piperazine (3.88 g, 38.70 mmol), 2-bromo, 5-fluoro benzotrifluoride (8.55 g, 35.18 mmol), tris(dibenzylidineacetone)dipalladium (0) (32.0 mg g, 0.35 mmol), rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (657.0 mg, 1.06 mmol) and sodium tert-butoxide (5.07 g, 52.77 mmol) were charged to a reaction flask. Toluene (40 mL) was introduced under nitrogen atmosphere and the reaction mixture was heated up at 110° C. for 5.0 hours. Reaction was complete as determined by TLC. The reaction mixture was diluted with dichloromethane, washed with water, saturated brine then dried over MgSO4 and concentrated. The crude product was purified via flash column chromatography to yield (R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazine as a light brown oil (3.1 g, 33.6% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07632838B2 |
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| Quelldatensatz | uspto-grants-2009_12 |
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| ORD ID | ord-9fadd48193674f86aee2834e1273fc9f |
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| Quellennotiz | uspto-grants-2009_12 |
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