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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1533113Erstellt: 24. Oktober 2026

Sodium Carbonate → 4-(4-Trifluoromethylphenyl)-1-indanone

https://huagongshe.com/de/reaction/1533113

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktTriphenylphosphineHCID 11776—
Edukt1-Indanone, 4-bromo-HCID 98713—
Edukt4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt4-(4-Trifluoromethylphenyl)-1-indanoneHCID 21702067—

Reaktionsschritte

6.33 g (0.03 mol) of 4-bromo-1-indanone and 5.7 g (0.03 mol) of 4-trifluoromethylphenylboronic acid are suspended with 6.36 g (0.06 mol) of sodium carbonate in a mixture of 100 ml of toluene with 20 ml of ethanol and 20 ml of water. Under an argon atmosphere, 320 mg (1.42 mmol) of palladium(II) acetate and 787 mg (3 mmol) of triphenylphosphine are added, and the mixture is boiled under reflux for 5 h. After the reaction is complete, the ethanol content is evaporated off in vacuo, 50 ml of 0.5 N sodium hydroxide solution are added to the residue, and the mixture is stirred and filtered with suction through a clarifying layer. The organic phase of the filtrate is separated off, shaken 3× with 50 ml of water each time, shaken once with saturated brine, dried over sodium sulfate and concentrated in vacuo. The crude product is chromatographed on silica gel with n-heptane/ethyl acetate 3/1. 4-(4-Trifluoromethylphenyl)-1-indanone is obtained with a melting point of 75-78° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06207689B1
Quelldatensatzuspto-grants-2001_03
ORD IDord-375b9fabe5db42ac91164e39087ad2d0
Quellennotizuspto-grants-2001_03