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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 539253Erstellt: 24. Oktober 2026

N-bromobutanimide → Benzene, 1,3-dibromo-2,4-dimethoxy-

https://huagongshe.com/de/reaction/539253

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-bromobutanimideHCID 67184—
Edukt2-Bromo-1,3-dimethoxybenzeneHCID 612296—
LösungsmittelAcetonitrileHCID 6342—
ProduktBenzene, 1,3-dibromo-2,4-dimethoxy-HCID 1164505395,1%

Reaktionsschritte

17.9 g of 1-bromo-2,6-dimethoxybenzene and 200 mL of acetonitrile were placed in a flask, and the resulting mixture was cooled on ice. Then, 14.7 g of N-bromosuccinimide was added. Then, while heating the reaction solution to room temperature, stirring was conducted for 8 hours. 2.39 g of N-bromosuccinimide was further added, and stirring was conducted at room temperature for 7 hours. After completion of the stirring, the solvent was distilled off under reduced pressure. Residues were dissolved in dichloromethane, and washed sequentially with sodium thiosulfate and saturated saline. An organic phase was dried with magnesium sulfate and concentrated. Residues were purified by means of silica gel column chromatography, whereby 23.2 g (yield: 95%) of colorless oil of 1,3-bromo-2,6-dimethoxybenzene was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08866135B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-a2a7e37766874d23abafe8067d25ed4d
Quellennotizuspto-grants-2014_10