HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205408Generated: November 1, 2026
Dimethylformamide → Methyl 1-methyl-1H-indole-5-carboxylate
https://huagongshe.com/reaction/2205408
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1H-Indole-5-Carboxylic Acid | HCID 74280 | — |
| Product | Methyl 1-methyl-1H-indole-5-carboxylate | HCID 10679201 | 93% |
Reaction Steps
A solution of 1H-indole-5-carboxylic acid (1.6 g, 10 mmol), sodium hydride (1.2 g, 30 mmol), iodomethane (6.2 mL, 100 mmol) and DMF (40 mL) was stirred and room temperature for 24 hr. The reaction mixture was then quenched with water (5 mL) and diluted with ether (150 mL) and ethyl acetate (50 mL). After washing with aq. NH4Cl (100 mL), water (100 mL) and then brine (100 mL), the organic layer was dried over MgSO4, filtered and concentrated. The remaining material was subjected to flash chromatography (ethyl acetate/hexane 1:4) to provide 1-methyl-1H-indole-5-carboxylic acid methyl ester as a crystalline solid (1.77 g, 93% yield). 1H NMR (400 MHz, CDCl3) δ 8.40 (s, 1H), 7.94 (d, 1H, J=9.0 Hz), 7.34 (d, 1H, J=9.0 Hz), 7.12 (d, 1H, J=2.9 Hz), 6.60 (d, 1H, J=2.9 Hz), 3.94 (s, 3H), 3.83 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09371281B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-afeeca0149064dfa848703f7483cc878 |
|---|
| Source note | uspto-grants-2016_06 |
|---|