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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1391726Erstellt: 26. Oktober 2026

Sodium Carbonate → 1-{6-[4-(Trifluoromethyl)phenyl]-2-pyridinyl}-1-pentanone

https://huagongshe.com/reaction/1391726

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
Edukt1-(6-Bromopyridin-2-yl)pentan-1-oneHCID 58629807—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt1-{6-[4-(Trifluoromethyl)phenyl]-2-pyridinyl}-1-pentanoneHCID 5862990194,8%

Reaktionsschritte

A solution of 1-(6-bromo-2-pyridinyl)-1-pentanone (2.51 g, 10.37 mmol) in DME (13 mL) was treated with 4-(triflouromethyl)benzeneboronic acid (2.36 g, 12.43 mmol), Pd(PPh3)4 (1.19 g, 1.03 mmol) and then a slurry of Na2CO3 (3.29 g, 31.04 mmol) in water (13 mL). The resulting mixture was then heated to reflux over 30 minutes and then stirred at this temperature for 17 hours. The mixture was then allowed to cool to rt and was reduced and the residue partitioned between EtOAc (200 mL) and water (200 mL). The aqueous was re-extracted with EtOAc (100 mL) and the combined organic layer washed with saturated aqueous NaHCO3 (250 mL), brine (250 mL), dried (MgSO4), filtered and reduced to give a brown orange solid residue. Purification by Biotage™ chromatography (silica) eluting with cyclohexane:EtOAc (gradient 1:0 to 10:1) afforded the title compound as a white solid (3.02 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07338960B2
Quelldatensatzuspto-grants-2008_03
ORD IDord-2323f8da141c47a6b4b89f7651ed89ba
Quellennotizuspto-grants-2008_03