HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 6-Chloro-1,2-dimethyl-1H-indole-3-carboxylic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | methyl 6-chloro-2-methyl-1H-indole-3-carboxylate | HCID 57443356 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-Chloro-1,2-dimethyl-1H-indole-3-carboxylic acid methyl ester | HCID 57443357 | 55.8% |
Reaction Steps
A mixture of 6-chloro-2-methyl-1H-indole-3-carboxylic acid methyl ester (2.76 g, 12.3 mmol), potassium carbonate (6.80 g, 49.2 mmol), iodomethane (1.07 mL, 17.2 mmol) and DMF (36 mL) is stirred overnight at room temperature. The mixture is diluted with ethyl acetate, washed twice with water, washed with brine and dried (MgSO4) and concentrated. The residue is triturated in 25 mL of 1:3 ethyl acetate-heptane and filtered to provide 1.63 g (55%) of pure title product. Additional material can be obtained through further trituration of the mother liquor. ES/MS m/e 238.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07846960B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-a725026dd39e47ea924ac6d0a3c206d1 |
| Source note | uspto-grants-2010_12 |