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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18179Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/18179

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktPhenolHCID 996—
EduktPotassium IodideHCID 4875—
EduktAmmonium HydroxideHCID 14923—
Edukt2-Bromo-4-methylphenolHCID 23109—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt2-Bromo-6-iodo-4-methylphenolHCID 59344907—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741326B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-46f8c0218ccc42b981649fe9bb0f79e4
Quellennotizuspto-grants-2010_06