HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 1-ethyl-6-methoxy-2-methyl-1H-indole-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-methoxy-2-methyl-1H-indole-3-carbonitrile | HCID 13904640 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-ethyl-6-methoxy-2-methyl-1H-indole-3-carbonitrile | HCID 59425265 | 92% |
Reaction Steps
To a suspension of NaH (0.6 g, 2 eq.) in DMF (7 mL) is added a solution of 6-methoxy-2-methyl-1H-indole-3-carbonitrile (1.3 g, 7.0 mmol) in DMF (8 mL) followed by ethyl iodide (1.2 mL, 2 eq.) at 0° C. After stirring for 1 h, the mixture is poured into ice water and then extracted with CH2Cl2. The organic layer is washed with brine and dried with Na2SO4. The solvent is evaporated under vacuum and purified with flash column chromatography on silica gel using EtOAc/petroleum ether (1/5) as eluent to yield 92% of 1-ethyl-6-methoxy-2-methyl-1H-indole-3-carbonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07868037B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-ff3633a85fb14e399d26b5a8775f5ede |
| Source note | uspto-grants-2011_01 |