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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1533114Erstellt: 26. Oktober 2026

Hydrogen Bromide → 2-Bromo-4-(4-trifluoromethylphenyl)-1-indanone

https://huagongshe.com/reaction/1533114

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen BromideHCID 260—
EduktBromineHCID 24408—
Edukt4-(4-Trifluoromethylphenyl)-1-indanoneHCID 21702067—
EduktSodium BisulfiteHCID 23665763—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Bromo-4-(4-trifluoromethylphenyl)-1-indanoneHCID 21702063—

Reaktionsschritte

2.76 g (10 mmol) of 4-(4-trifluoromethylphenyl)-1-indanone are dissolved in 20 ml of glacial acetic acid and, after addition of 10 μl of a 48% strength solution of HBr in glacial acetic acid, while stirring a solution of 0.516 ml (10.05 mmol) of bromine in glacial acetic acid is added. After 3 h at room temperature, the reaction mixture is poured into a mixture of 100 ml of water with 100 g of ice and 100 mg of sodium bisulfite, and the resulting suspension is shaken with dichloromethane. The organic phase is washed 3× with water, dried over sodium sulfate, filtered and concentrated in vacuo. The residue is chromatographed on silica gel with dichloromethane/n-heptane 3/1. 2-Bromo-4-(4-trifluoromethylphenyl)-1-indanone is obtained with a melting point of 102-105° C., in addition to a little 2,2-dibromo compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06207689B1
Quelldatensatzuspto-grants-2001_03
ORD IDord-efcc472b911d42ab97775ba7c45dcc8e
Quellennotizuspto-grants-2001_03