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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 683Erstellt: 24. Oktober 2026

4-Piperidone → 1-(2-Chloro-4-fluorophenyl)piperidin-4-one

https://huagongshe.com/de/reaction/683

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-PiperidoneHCID 33721—
Edukt1-Bromo-2-chloro-4-fluorobenzeneHCID 2733406—
ReagenzSodium t-butoxideHCID 23676156—
KatalysatorPalladium (II) acetateHCID 4144353—
Katalysator2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
LösungsmittelTolueneHCID 1140—
Produkt1-(2-Chloro-4-fluorophenyl)piperidin-4-oneHCID 290802910%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

To a round bottom flask was added palladium(II) acetate (0.012 g, 0.06 mmol), dicyclohexyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (0.026 g, 0.06 mmol), and sodium tert-butoxide (0.213 g, 2.21 mmol). Added 5 mL toluene/t-butanol mix and purged with nitrogen. Added piperidin-4-one (0.15 g, 1.11 mmol), in 3 mL tol/tbuoh (slurry), followed by 1-bromo-2-chloro-4-fluorobenzene (0.255 g, 1.22 mmol), in 2 mL tol/tbuoh. Flushed with additional nitrogen and then heated to 120oC overnight. Let reaction mixture cool to room temperature and filtered through Celite. Rinsed repeatedly with EtOAc and concentrated in vacuo. Purified via ISCO 12g SiO2 column using 0-20% hexanes/ethyl acetate. Fractions 19 and 20 were combined and concentrated to afford a white solid. NMR (I200805922.42) shows a mess. Discarded. Will try another way.

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-5c5d7fac90d14102bcad7fe6bdad56a8
Quellennotiz750 AstraZeneca ELN dataset