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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1526949Erstellt: 26. Oktober 2026

Dimethyl Sulfoxide → ethyl 2-methyl-1H-indole-3-carboxylate

https://huagongshe.com/reaction/1526949

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktEthyl AcetoacetateHCID 8868—
EduktCesium carbonateHCID 10796—
Edukt2-IodoanilineHCID 11995—
KatalysatorHCID 178419072HCID 178419072—
LösungsmittelWaterHCID 962—
Produktethyl 2-methyl-1H-indole-3-carboxylateHCID 407235815,1%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a mixed solution of dimethyl sulfoxide and water (20 mL), 2-iodobenzenamine (3.0 g, 13.7 mmol), ethyl 3-oxobutanoate (2.0 g, 15.1 mmol), copper(I) oxide (0.2 g, 1.4 mmol) and cesium carbonate (4.5 g, 13.7 mmol) was added. The mixture was stirred at 100° C. for 9 hours under nitrogen gas atmosphere. The reaction mixture was filtered through a pad of celite. The filtrate was diluted with water and extracted with ethyl acetate. The organic phase was concentrated in vacuo, and then the residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=5:1) to give ethyl 2-methyl-1H-indole-3-carboxylate as a light yellow solid (0.42 g, 15%). 1H NMR (300 MHz, CDCl3): δ 8.12-8.09 (m, 1H), 7.31-7.16 (m, 3H), 4.40 (q, J=6.9 Hz, 2H), 2.77 (s, 3H), 1.45 (t, J=6.9 Hz, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09085583B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-bb1e46f6229547b2979abf4b7300b792
Quellennotizuspto-grants-2015_07