HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-Fluoro-1,3-dimethyl-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Fluoro-3-methyl-1H-indole | HCID 22351503 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Fluoro-1,3-dimethyl-1H-indole | HCID 18729676 | 78.6% |
Reaction Steps
To a solution of 5-fluoro-3-methyl-indole (CAS: 392-13-2, 2.5 g) in DMF (20 ml) was added potassium hydroxide (1.41 g). The suspension was stirred at rt for 1 h and iodomethane (2.85 g) was added dropwise at 0-5° C. The reaction mixture was stirred at rt for 18 h and concentrated under high vacuum. The residue was quenched with water and extracted with ethyl acetate. The organics were washed, dried and concentrated. The crude residue was chromatographed on silica gel using heptane/ethyl acetate as eluent to obtain the desired compound (2.15 g) as a colorless liquid. MS (EI): 163.1 (M)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158655B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-fe867d1c5709445e8feefb28b0b4905f |
| Source note | uspto-grants-2012_04 |