HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526949Generated: October 25, 2026
Dimethyl Sulfoxide → ethyl 2-methyl-1H-indole-3-carboxylate
https://huagongshe.com/reaction/1526949
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Iodoaniline | HCID 11995 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | Water | HCID 962 | — |
| Product | ethyl 2-methyl-1H-indole-3-carboxylate | HCID 4072358 | 15.1% |
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, 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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09085583B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-bb1e46f6229547b2979abf4b7300b792 |
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| Source note | uspto-grants-2015_07 |
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