Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 2-Bromophenol | HCID 7244 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Bromoanisole | HCID 11358 | — |
Reaction Steps
Into a three-necked flask of 1liter, 25g (0.145 mol) of o-bromophenol, 6.1 g (0,152mol) of sodium hydroxide and 300 ml of ethanol were charged and refluxed for two hours. Then, 82.0 g (0.578 mol) of methyl iodide was added dropwise and the mixture was refluxed further for four hours. After the mixture was cooled to room temperature, 600 ml of diethyl ether was added. The mixture was charged into a separatory funnel. Separated organic layer was washed successively with, 100 ml of 2N-hydrochloric acid cooled with ice, 300 ml of saturated sodium thiosulfate, and water until the washings were neutral. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The concentrate was distilled under reduced pressure to obtain 25.3 g (0.135 mol) of o-methoxyphenylbromide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05395766 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-15af841dab684444b99547c16e152820 |
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| Source note | uspto-grants-1995_03 |
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