HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773975Generated: November 2, 2026
Methyl iodide → Methyl 2-(3-bromo-2-methoxyphenyl)acetate
https://huagongshe.com/reaction/1773975
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 2-(3-bromo-2-hydroxyphenyl)acetate | HCID 12159074 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2-(3-bromo-2-methoxyphenyl)acetate | HCID 66643982 | — |
Reaction Steps
To a solution of (3-bromo-2-hydroxy-phenyl)-acetic acid methyl ester (866 mg, 3.5 mmol, 1 eq.) and potassium carbonate (2.44 g, 17.7 mmol, 5 eq.) in MeCN (9 mL), iodomethane (0.67 mL, 10.6 mmol, 3 eq.) was added. The resulting mixture was stirred at 50° C. for 2 hours. The reaction mixture was diluted with AcOEt and water. The layers were separated and the aq. phase was extracted with AcOEt (2×). The comb. org. layers were dried over MgSO4, filtered, and concentrated in vacuo to give the title compound as an orange oil. The product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09255090B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-059b8d3803e1430a89e83f9f1a70f243 |
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| Source note | uspto-grants-2016_02 |
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