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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11405Erstellt: 23. Oktober 2026

Dimethylformamide → methyl 2-methyl-1H-indole-4-carboxylate

https://huagongshe.com/de/reaction/11405

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
Edukt1-(4-(2-Propyloxyethoxy)benzoyl)-2-methylindole-4-acetic AcidHCID 21974383—
EduktHCID 178418416HCID 178418416—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produktmethyl 2-methyl-1H-indole-4-carboxylateHCID 11769304—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of 2-methyl-4-trifluoromethanesulfoxyindole (6.32 g; prepared in Reference Example 1) in methanol (33.43 ml)-N,N-dimethylformamide (200 ml) was added triethylamine (6.3 ml) and tetrakis(triphenylphosphine)palladium (2.6 g). The inside of the vessel was replaced with carbon monoxide and the mixture was stirred at 60° C. overnight. After the reaction was completed, to the mixture was added water and ethyl acetate and then the mixture was extracted. The aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with water and a saturated aqueous solution of sodium chloride, successively, dried and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (n-hexane-ethyl acetate) to give the title compound (4.29 g) having the following physical data.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07098234B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-0da4b96c7f31489a97331b969fe85f03
Quellennotizuspto-grants-2006_08