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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1610784Erstellt: 25. Oktober 2026

2-Bromonaphthalene → 2-Bromo-9,10-di-naphthalene-2-yl-9,10-dihydro-anthracene-9,10-diol

https://huagongshe.com/reaction/1610784

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromonaphthaleneHCID 11372—
Edukt2-BromoanthraquinoneHCID 221013—
EduktHCID 178418306HCID 178418306—
LösungsmittelPentaneHCID 8003—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Bromo-9,10-di-naphthalene-2-yl-9,10-dihydro-anthracene-9,10-diolHCID 2224716693%

Reaktionsschritte

To a solution of 2-bromonaphthalene (6.49 g, 31.3 mmol) in dry THF (50 ml) was added dropwise t-BuLi (18.4 ml of a 1.7 M solution in pentane) at −78° C. under nitrogen. After the mixture had been stirred for 30 min, 2-bromoanthraquinone (3.00 g, 10.4 mmol) was added at −78° C. The cooling bath was removed and the mixture was stirred for 2 hours at room temperature. The mixture was quenched with saturated aqueous ammonium chloride solution (50 ml) and extracted with ethyl ether (3×50 ml). The combined organic extracts were dried over MgSO4 and concentrated under vacuum. The crude product was slurried in petroleum ether, filtered off with suction, and washed with petroleum ether. After drying, the 2-bromo-9,10-di-naphthalene-2-yl-9,10-dihydro-anthracene-9,10-diol (5.30 g, 93%) was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06984462B2
Quelldatensatzuspto-grants-2006_01
ORD IDord-e36c353889f04976be3e3322e335d23f
Quellennotizuspto-grants-2006_01