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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 857421Erstellt: 24. Oktober 2026

Sodium hydride → Ethyl 4-bromo-6-fluoro-2-(methoxycarbonyl)-1H-indole-1-butanoate

https://huagongshe.com/de/reaction/857421

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
EduktEthyl 4-bromobutyrateHCID 76300—
EduktMethyl 4-bromo-6-fluoro-1H-indole-2-carboxylateHCID 21867463—
KatalysatorTetrabutylammonium IodideHCID 67553—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl 4-bromo-6-fluoro-2-(methoxycarbonyl)-1H-indole-1-butanoateHCID 2186755792,9%

Reaktionsschritte

To a solution of methyl 4-bromo-6-fluoro-1H-indole-2-carboxylate (10 g, 36.8 mmol) in DMF (100 mL) at 0° C. was added NaH (1.8 g, 44.2 mmol, 60% in oil). The mixture was stirred at r.t. for 30 minutes and tetra-n-butylammonium iodide (500 mg) was added, followed by the addition of ethyl 4-bromobutyrate (10.1 g, 51.5 mmol). The reaction mixture was stirred at r.t. for 3 h, poured into saturated aqueous NH4Cl and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4 and concentrated. The residue was purified by silica gel chromatography eluted with 20% EtOAc to give 13.2 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07144913B2
Quelldatensatzuspto-grants-2006_12
ORD IDord-1cb1a896013746d3859385f2d7568f03
Quellennotizuspto-grants-2006_12