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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1868119Erstellt: 26. Oktober 2026

2-Bromo-5-fluorobenzotrifluoride → (R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazine

https://huagongshe.com/reaction/1868119

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromo-5-fluorobenzotrifluorideHCID 520983—
Edukt2-Methylpiperazine, (R)-HCID 7330434—
EduktSodium t-butoxideHCID 23676156—
KatalysatorBinap, (A+-)-HCID 634876—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
Produkt(R)-1-(4-fluoro-2-(trifluoromethyl)phenyl)-3-methylpiperazineHCID 6855494882,4%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

(R)-2-methyl-piperazine (3.5 g, 34.9 mmol), 2-bromo-5-fluoro benzotrifluoride (7.74 g, 31.7 mmol), BINAP (0.59 g, 0.95 mmol), tBuONa (4.58 g, 47.65 mmol) and Pd2(dba)3 (0.29 g, 0.32 mmol) were mixed in the flask and purged with N2. Anhydrous toluene (50 mL) was added and purged with N2 again. The resulting mixture was heated in an oil bath at 100° C. under N2 for 3 hours. The mixture was cooled to room temperature, diluted with dichloromethane (150 mL), washed with H2O (30 mL) first, then washed with saturated brine (30 mL). The combined organic layer was dried over Na2SO4, concentrated down under reduced pressure to give a brown color liquid as crude. The crude product was purified on silica gel column eluted with 5-10% MeOH in DCM to give (3R)-1-[4-fluoro-2-(trifluoromethyl)phenyl]-3-methylpiperazine as a light yellow oil (6.85 g, 82%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07632838B2
Quelldatensatzuspto-grants-2009_12
ORD IDord-d533b43a677146f8923ac74e7be809ee
Quellennotizuspto-grants-2009_12