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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11405Generated: October 26, 2026

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

https://huagongshe.com/reaction/11405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
Reactant1-(4-(2-Propyloxyethoxy)benzoyl)-2-methylindole-4-acetic AcidHCID 21974383—
ReactantHCID 178418416HCID 178418416—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Productmethyl 2-methyl-1H-indole-4-carboxylateHCID 11769304—

Reaction Conditions

Temperature60 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07098234B2
Source datasetuspto-grants-2006_08
ORD IDord-0da4b96c7f31489a97331b969fe85f03
Source noteuspto-grants-2006_08