HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 1-[1-(3-Fluorophenyl)-3-methyl-1H-indol-2-yl]ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 1-(3-Fluorophenyl)-N-methoxy-N,3-dimethyl-1H-indole-2-carboxamide | HCID 58565338 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[1-(3-Fluorophenyl)-3-methyl-1H-indol-2-yl]ethanone | HCID 58565366 | 71% |
Reaction Steps
To a mixture of 1-(3-fluorophenyl)-N-methoxy-N,3-dimethyl-1H-indole-2-carboxamide (0.27 g, 0.86 mmol) in tetrahydrofuran (5 mL) was added 3.0 M methylmagnesium bromide in ether (2.3 mL, 6.9 mmol). The reaction was stirred at room temperature overnight. The reaction was quenched with saturated NH4Cl solution and extracted with EtOAc. The combined organic layers were dried over MgSO4, concentrated, and purified on silica gel (eluting with 0-15% EtOAc/hexane) to give the desired product (0.165 g, 71%). LCMS calculated for C17H15FNO(M+H)+: m/z=268.1. Found: 268.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062055B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-8eeeba7412334b53812c18052e6d8137 |
| Source note | uspto-grants-2015_06 |