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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 338391Erstellt: 25. Oktober 2026

Potassium Carbonate → 2-[4-(6-chloro-3-formyl-1H-indol-5-yl)phenoxy]acetamide

https://huagongshe.com/reaction/338391

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt2-(4-Bromophenoxy)acetamideHCID 302864—
Edukt6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indoleHCID 86698733—
KatalysatorBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
LösungsmittelDimethylformamideHCID 6228—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-[4-(6-chloro-3-formyl-1H-indol-5-yl)phenoxy]acetamideHCID 8669873476%

Reaktionsschritte

A mixture of 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole (260 mg, 1.00 mmol) and N,N-dimethylformiminium chloride (250 mg, 2.00 mmol) in dry 1,4-dioxane (5 mL) and DMF (1 mL) was sealed in a reaction vessel and stirred at room temperature for 10 minutes to give a white slurry. To the slurry was added 2M aqueous potassium carbonate (2.5 mL, 5 mmol), 2-(4-bromophenoxy)acetamide (240 mg, 1.00 mmol) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (50 mg). The sealed vial was degassed with nitrogen and heated to 90° C. for 30 minutes. The reaction was quenched with water (20 mL), and extracted with EtOAc (3×20 mL). The combined organic layers were dried and concentrated in vacuo to give 2-[4-(6-chloro-3-formyl-1H-indol-5-yl)phenoxy]acetamide (250 mg, 55% yield) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889730B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-554af53e4f9949389bb5a098541b43aa
Quellennotizuspto-grants-2014_11