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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608477Generated: October 30, 2026

Ethanol → 2-Bromoanisole

https://huagongshe.com/reaction/1608477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethyl iodideHCID 6328—
Reactant2-BromophenolHCID 7244—
ReactantSodium HydroxideHCID 14798—
SolventDiethyl EtherHCID 3283—
Product2-BromoanisoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05395766
Source datasetuspto-grants-1995_03
ORD IDord-15af841dab684444b99547c16e152820
Source noteuspto-grants-1995_03