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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
Eduktalpha,alpha,alpha,3-TetrafluorotolueneHCID 67867—
Edukt2-Methylpiperazine, (R)-HCID 7330434—
EduktSodium t-butoxideHCID 23676156—
KatalysatorBinap, (A+-)-HCID 634876—
LösungsmittelDichloromethaneHCID 6344—
Produkt(R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazineHCID 6855494833,6%

Reaktionsbedingungen

Temperatur110 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07632838B2
Quelldatensatzuspto-grants-2009_12
ORD IDord-9fadd48193674f86aee2834e1273fc9f
Quellennotizuspto-grants-2009_12