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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1698737Erstellt: 25. Oktober 2026

Bromochloromethane → 2-Bromo-4-methoxy-8,9-dihydro-5,7-dioxabenzocycloheptene

https://huagongshe.com/reaction/1698737

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromochloromethaneHCID 6333—
EduktAmmonium ChlorideHCID 25517—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt4-Bromo-2-(2-hydroxyethyl)-6-methoxyphenolHCID 67097474—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-Bromo-4-methoxy-8,9-dihydro-5,7-dioxabenzocyclohepteneHCID 5951721344,6%

Reaktionsschritte

To a solution of 898 mg of 4-bromo-2-(2-hydroxyethyl)-6-methoxyphenol in 10 ml of DMF there was added 1 g of sodium bistrimethylsilylamide while cooling on ice, and the mixture was stirred at room temperature for 30 minutes. After adding 1 ml of bromochloromethane to the reaction mixture, it was stirred at 80° C. for 20 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 (420 mg) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08163787B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-b08c5e3e2d14475bbd5993c6852eadb7
Quellennotizuspto-grants-2012_04