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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1816726Erstellt: 26. Oktober 2026

Sodium Methoxide → 5-Bromo-2-(7-methoxyheptyloxy)-1,3-dimethylbenzene

https://huagongshe.com/reaction/1816726

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium MethoxideHCID 10942334—
Edukt5-Bromo-2-(7-bromoheptyloxy)-1,3-dimethylbenzeneHCID 22494636—
LösungsmittelMethanolHCID 887—
Produkt5-Bromo-2-(7-methoxyheptyloxy)-1,3-dimethylbenzeneHCID 22494771—

Reaktionsschritte

A solution of crude 5-bromo-2-(7-bromoheptyloxy)-1,3-dimethylbenzene (7.81 g) in methanol (78 ml) was treated with 28% sodium methoxide in methanol (78 ml), and the solution was refluxed for 8 hours. After cooling, the reaction mixture was evaporated under reduced pressure, and the residue was extracted with methylene chloride. The organic layer was dried over magnesium sulfate and magnesium sulfate was filtered off, and then the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography eluting with a mixed solvent of n-hexane-ethyl acetate (from 0% to 7% gradient elution) to give 5-bromo-2-(7-methoxyheptyloxy)-1,3-dimethylbenzene (3.34 g) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06884868B1
Quelldatensatzuspto-grants-2005_04
ORD IDord-f2cfa733b5be49458a48c3a789d932ac
Quellennotizuspto-grants-2005_04