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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-(3-bromo-2-hydroxyphenyl)acetateHCID 12159074—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-(3-bromo-2-methoxyphenyl)acetateHCID 66643982—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255090B2
Source datasetuspto-grants-2016_02
ORD IDord-059b8d3803e1430a89e83f9f1a70f243
Source noteuspto-grants-2016_02