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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 551Erstellt: 24. Oktober 2026

Piperidine → 3-Chloro-4-(piperidin-1-yl)benzoic acid

https://huagongshe.com/de/reaction/551

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperidineHCID 8082—
Edukt4-Bromo-3-chlorobenzoic acidHCID 12594302—
ReagenzSodium t-butoxideHCID 23676156—
KatalysatorBinap, (A+-)-HCID 634876—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelTolueneHCID 1140—
Produkt3-Chloro-4-(piperidin-1-yl)benzoic acidHCID 1895623110%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

4-bromo-3-chlorobenzoic acid (0.353 g, 1.5 mmol), piperidine (0.234 mL, 2.25 mmol), and sodium tert-butoxide (0.216 g, 2.25 mmol) were stirred together under N2 and heated to 80 °C. Pd2(dba)3 (0.014 g, 0.015 mmol), and BINAP (0.031 g, 0.05 mmol) were mixed in toluene (2 mL) and then added to the mixture and stirred at 110 °C overnight. LCMS showed a very small amount of desired product (~2%). The reaction mixture was degassed with N2 for 30 minutes, then addtional Pd/ Binap was added. The reaction was again heated to 110 C. LCMS showed a small amount of desired product (~10%) but mostly still starting material. The desired product was not isolated from this reaction.

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-398e791076cd44778e3b80090d8d8371
Quellennotiz750 AstraZeneca ELN dataset