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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131641Erstellt: 25. Oktober 2026

Ethyl Acetate → Ethyl 5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/131641

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Edukt3-Fluorobenzyl chlorideHCID 9974—
EduktPotassium CarbonateHCID 11430—
Eduktethyl 5-fluoro-1H-indole-2-carboxylateHCID 2727899—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl 5-fluoro-1-(3-fluorobenzyl)-1H-indole-2-carboxylateHCID 5743151461,8%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A suspension of 0.207 g (1 mmol) of ethyl 5-fluoro-1H-indole-2-carboxylate, 0.173 g (1.2 mmol) of 3-fluorobenzyl chloride and 0.276 g (2 mmol) of potassium carbonate in 10 ml of dimethylformamide is stirred at 60° C. for 24 hours. The reaction mixture is subsequently cooled and is poured into a mixture of ice-cold water and of ethyl acetate. After settling, the organic phase is separated and then it is washed with two times 50 ml of water and then with 50 ml of a saturated sodium chloride solution. The solution is dried over magnesium sulfate and is filtered, and then the filtrate is concentrated under reduced pressure. 0.195 g of an oil is obtained, which oil is used as is in the following stage.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384969B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-276fbec6c06f45fea6c86055a2670eef
Quellennotizuspto-grants-2008_06