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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 14454Erstellt: 25. Oktober 2026

Chlorotrimethylsilane → Ethanone, 2-bromo-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-

https://huagongshe.com/reaction/14454

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotrimethylsilaneHCID 6397—
EduktBromineHCID 24408—
Edukt1-(2,2-Dimethyl-2,4-dihydro-1,3-benzodioxin-6-yl)ethan-1-oneHCID 21880610—
EduktSodium hexamethyidisilazaneHCID 45051731—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthanone, 2-bromo-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-HCID 11150315—

Reaktionsschritte

To the product of step (b) (23.4 g, 0.113 mol) in 600 mL of THF at −78° C. was added 135 mL of 1.0 M sodium hexamethyldisilazane in THF (Sigma-Aldrich). After 1 hour, trimethylsilyl chloride (15.8 mL, 0.124 mol) was added. After another 30 minutes, bromine (5.82 mL, 0.113 mol) was added. After 10 minutes, the reaction was quenched by diluting the reaction mixture with diethyl ether and pouring it onto 500 mL of 5% aqueous Na2SO3 premixed with 500 mL of 5% aqueous NaHCO3. The phases were separated and the organic phase was washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to give the title compound as an oil that solidified upon storage in the freezer.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732441B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-ef4ea43a78ff495cb8c3230a83042d2f
Quellennotizuspto-grants-2010_06