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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18179Generated: October 25, 2026

Iodine → 2-Bromo-6-iodo-4-methylphenol

https://huagongshe.com/reaction/18179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPhenolHCID 996—
ReactantPotassium IodideHCID 4875—
ReactantAmmonium HydroxideHCID 14923—
Reactant2-Bromo-4-methylphenolHCID 23109—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-Bromo-6-iodo-4-methylphenolHCID 59344907—

Reaction Conditions

Temperature60 °C

Reaction Steps

2-Bromo-4-methylphenol (10.11 gm, 54.05 mmol) was mixed with concentrated ammonium hydroxide (50 ml) and methanol (20 ml). Potassium iodide (17.94 g, 108 mmol), iodine (13.72 g, 54.05 mmol) and water (60 ml) were mixed to give a dark brown solution which was added in portions to the phenol solution. Additional methanol (200 ml) was added in portions as precipitating product made the mixture too viscous to stir. When all the iodine solution had been added the mixture was heated to 60° C. till the brown color faded. The mixture was cooled, filtered and the solid rinsed three times with water. The solid was dissolved in dichloromethane, dried over magnesium sulfate, filtered and stripped to give 2-Bromo-4-methyl-6-iodophenol as an oil that crystallized on standing. The filtrate and water rinses were concentrated and extracted twice with ethyl acetate, dried over magnesium sulfate, filtered and stripped to give additional 2-bromo-4-methyl-6-iodophenol for a total of 16.24 g, 96% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741326B2
Source datasetuspto-grants-2010_06
ORD IDord-46f8c0218ccc42b981649fe9bb0f79e4
Source noteuspto-grants-2010_06