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HRID 61802Erstellt: 24. Oktober 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 3-Bromo-9-methoxy-6,6-dimethyl-5,6-dihydro-benzo[b]carbazol-11-one

https://huagongshe.com/de/reaction/61802

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
EduktEthyl AcetateHCID 8857—
Edukt3-Bromophenylhydrazine hydrochlorideHCID 33757—
Edukt6-Methoxy-1,1-dimethyl-3,4-dihydronaphthalen-2-oneHCID 12561944—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
Produkt3-Bromo-9-methoxy-6,6-dimethyl-5,6-dihydro-benzo[b]carbazol-11-oneHCID 6683452046%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

6-Methoxy-1,1-dimethyl-3,4-dihydro-1H-naphthalen-2-one (Compound J2, 2.15 g, 10.5 mmol) and 3-bromophenylhydrazine hydrochloric acid salt (3.11 g, 1.3 eq.) were dissolved in acetic acid (12 mL), and stirred at 100° C. for 2.5 hr under nitrogen atmosphere. After cooling, the reaction solution was added with ethyl acetate, washed with water, saturated aqueous solution of sodium hydrogen carbonate, and saturated brine, and dried over magnesium sulfate. After the filtration, it was concentrated under reduced pressure. The resulting residues were dissolved in THF (30 mL) and water (3 mL), added with DDQ (5.96 g, 2.5 eq.) at 0° C., and then stirred at room temperature overnight. The reaction solution was added with MTBE, washed with 0.5 N aqueous solution of sodium hydroxide and saturated brine, and dried over magnesium sulfate. After filtration and the concentration under reduced pressure, the resulting residues were washed with MTBE to obtain the title compound (brown solid, 1.80 g, 46%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440922B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-4c3f07123dfe4df0ae246339a8f3665c
Quellennotizuspto-grants-2016_09