HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Ethyl 4-benzyloxy-1-methylindole-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4-(phenylmethoxy)-1H-indole-2-carboxylate | HCID 119707 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 4-benzyloxy-1-methylindole-2-carboxylate | HCID 22054863 | — |
Reaction Steps
To a stirred suspension of sodium hydride (0.27 g, 60% dispersion in mineral oil) in DMF (50 mL) under nitrogen at room temperature was added ethyl 4-benzyloxyindole-2-carboxylate (1.59 gm). Methyl iodide (0.5 mL) was added 10 min. later. After 2 hr. excess sodium hydride was quenched with acetic acid (0.4 mL) and the solvent evaporated under reduced pressure. The residue was taken into EtOAc, washed with water and brine, dried over MgSO4, and evaporated to dryness to give an oil which was triturated with hexane to precipitate 1.45 g of the title compound. Mp 89-90.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07402604B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-1aa8a9db03b541abab1cb95525cf4d22 |
| Source note | uspto-grants-2008_07 |