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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1043887Erstellt: 26. Oktober 2026

Benzoyl Peroxide → 2-Bromo-5-(methoxymethyl)-1,3-dimethylbenzene

https://huagongshe.com/reaction/1043887

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
Edukt2-BromomesityleneHCID 68473—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt2-Bromo-5-(methoxymethyl)-1,3-dimethylbenzeneHCID 8668632615,4%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

2-bromomesitylene (5.00 g) was dissolved in carbon tetrachloride (50 mL). NBS (4.45 g) and benzoyl peroxide (182 mg) were added to the solution, and the mixture was stirred at 80° C. for three hours. The reaction mixture was returned to room temperature and filtered. The solid collected by filtration was washed with n-heptane. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (n-heptane). The resulting fraction was concentrated under reduced pressure. The residue was dissolved in THF (120 mL). Sodium methoxide (28% solution in methanol, 9.35 mL) was added to the solution, and the mixture was stirred at 80° C. for four hours. The reaction mixture was returned to room temperature and concentrated under reduced pressure. Water was added to the residue, followed by extraction with DCM. The organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/n-heptane, 0% to 5%). The resulting fraction was concentrated under reduced pressure, and the residue was purified again by NH silica gel column chromatography (n-heptane) to give the title compound (880 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08563565B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-9012ecba62c0433ab5a891e812fdb66d
Quellennotizuspto-grants-2013_10