HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Methyl 4-chloro-1,2-dimethyl-1H-indole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | methyl 4-chloro-2-methyl-1H-indole-3-carboxylate | HCID 59473719 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | Methyl 4-chloro-1,2-dimethyl-1H-indole-3-carboxylate | HCID 59473668 | 72% |
Reaction Steps
Methyl 4-chloro-2-methyl-1H-indole-3-carboxylate (13.45 mmol, 1.0 equiv.) was dissolved in DMF (7 ml) and added at 0° C. to a suspension of NaH (26.90 mmol, 2.0 equiv.) in DMF (13 ml). The mixture was then stirred for 30 min. Methyl iodide (20.17 mmol, 1.5 equiv.) was added dropwise at 0° C. and stirring was carried out for 2 h at 25° C. The reaction mixture was diluted with NH4Cl solution (20 ml) and extracted with ethyl acetate (3×50 ml). The combined organic phases were washed with water and sat. NaCl solution (in each case 50 ml), dried over Na2SO4 and concentrated to dryness under reduced pressure. Yield: 72%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492559B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-7daa7349e05845bdb1ec6c47cb131807 |
| Source note | uspto-grants-2013_07 |