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HRID 1220Erstellt: 23. Oktober 2026

Benzoyl Peroxide → 4,6-Dibromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/de/reaction/1220

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
Edukt1,2-DibromonaphthaleneHCID 226291—
Edukt6-Bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene naphthaleneHCID 19694976—
Produkt4,6-Dibromo-1,1-dimethyl-1,2,3,4-tetrahydronaphthaleneHCID 19694961—

Reaktionsschritte

Employing the above-described procedure for the conversion of 6-bromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene naphthalene (Compound F) to the dibromonaphthalene derivative (Compond I), 3.5 g (14.6 mmol) of (Compound F), 2.86 g (16.1 mmol) of N-bromosuccinimide and 150 mg (0.62 mmol ) of benzoylperoxide gave crude 4,6-dibromo-1,2,3,4-tetrahydro-1,1-dimethylnaphthalene (Compound I). To a solution of this crude dibromonaphthalene derivative (Compound I) in 50 ml of THF was added 5.38 g (47.1 mmol) of potassium thioacetate. The mixture was refluxed for 6 hours under argon atmosphere, filtered through celite and concentrated in vacuo. Purification by chromatography (silica, 10% EtOAc-hexane) yielded the title compound as red oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723620
Quelldatensatzuspto-grants-1998_03
ORD IDord-0a6411cd1b2143cf95c4b57b2c8fb6d3
Quellennotizuspto-grants-1998_03