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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206464Generated: October 30, 2026

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

https://huagongshe.com/reaction/2206464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantEthyl AcetoacetateHCID 8868—
ReactantCesium carbonateHCID 10796—
Reactant2-IodoanilineHCID 11995—
CatalystHCID 178419072HCID 178419072—
SolventWaterHCID 962—
Productethyl 2-methyl-1H-indole-3-carboxylateHCID 407235815.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

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, CDCl_): 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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371331B2
Source datasetuspto-grants-2016_06
ORD IDord-d7d7446a198e4541af711df947a61511
Source noteuspto-grants-2016_06