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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 338221Erstellt: 25. Oktober 2026

Potassium Carbonate → 6-Chloro-5-phenyl-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/338221

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktPhenylboronic AcidHCID 66827—
Edukt5-bromo-6-chloro-1H-indole-3-carbaldehydeHCID 86698566—
KatalysatorBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
LösungsmittelEthanolHCID 702—
LösungsmittelTolueneHCID 1140—
Produkt6-Chloro-5-phenyl-1H-indole-3-carbaldehydeHCID 8669857298%

Reaktionsschritte

A mixture of 5-bromo-6-chloro-1H-indole-3-carbaldehyde (200 mg, 0.77 mmol), phenyl boronic acid (114 mg, 0.93 mmol), 2N aqueous potassium carbonate (1.15 mL, 3.10 mmol) in toluene (3.3 mL) and EtOH (1.1 mL) was degassed with N2, treated with [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (56.6 mg, 0.077 mmol), and degassed again with N2. The mixture was subjected to microwave irradiation conditions at 120° C. for 30 minutes. The reaction mixture was cooled to room temperature, diluted with water and extracted with EtOAc (50 mL). The organic layer was washed with brine, dried over MgSO4 and concentrated in vacuo. The crude material was purified by flash chromatography (0-46% EtOAc/petroleum ether) to afford the title compound (190 mg, 98% yield) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889730B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-bc14fd9a3671457d8e8bfb84eb9723b6
Quellennotizuspto-grants-2014_11