HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-Bromo-1,3-dimethoxy-5-(1-methoxyethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(4-Bromo-3,5-dimethoxyphenyl)ethanol | HCID 58223484 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-1,3-dimethoxy-5-(1-methoxyethyl)benzene | HCID 58223419 | — |
Reaction Steps
To a tetrahydrofuran (100 mL) solution of 1-(4-bromo-3,5-dimethoxyphenyl)ethanol (7.24 g, 27.7 mmol) was added sodium hydride (1.33 g, 33.2 mmol) at 0° C., and the mixture was stirred for 10 minutes. To the mixture was added dropwise iodomethane (1.90 mL, 30.5 mmol), and the mixture was stirred at room temperature for one hour. After the reaction was completed, water was added to the reaction mixture while cooling on ice, which was extracted with ethyl acetate and dried over anhydrous magnesium sulfate, and the solvent was then distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-heptane/ethyl acetate: 10/1 then 1/4) to obtain the title compound (7.39 g, 26.9 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530504B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-9661cd9f131b4feca1184662d0f3fc1a |
| Source note | uspto-grants-2013_09 |