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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1161403Erstellt: 24. Oktober 2026

Sodium Iodide → 6-bromo-8-methoxy-4H-benzo[1,3]dioxine

https://huagongshe.com/de/reaction/1161403

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktBromochloromethaneHCID 6333—
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
Edukt4-Bromo-2-(hydroxymethyl)-6-methoxyphenolHCID 894092—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt6-bromo-8-methoxy-4H-benzo[1,3]dioxineHCID 59511816—

Reaktionsschritte

To a solution of the 50 g of 4-bromo-2-hydroxymethyl-6-methoxyphenol in 450 ml of DMF there was added 20 g of sodium hydride (60% oily suspension) while cooling on ice, and the mixture was stirred at room temperature for 30 minutes. After adding 15 ml of bromochloromethane and 3.2 g of sodium iodide to the reaction mixture, it was stirred at 80° C. for 6 hours under a nitrogen atmosphere. Saturated aqueous ammonium chloride was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (31.2 g) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07816522B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-35177c5cae3644e08b04824dbc65f47b
Quellennotizuspto-grants-2010_10