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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 321919Erstellt: 24. Oktober 2026

Water → 1-(4,7-Dimethyl-1-indenyl)-2-(4,7-dimethyl-1-indenyl)methyl benzene

https://huagongshe.com/de/reaction/321919

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4,7-dimethyl-1H-indeneHCID 81458—
EduktButyllithiumHCID 178418339—
LösungsmittelHexaneHCID 8058—
LösungsmittelTetrahydrofuran hexaneHCID 21883165—
Produkt1-(4,7-Dimethyl-1-indenyl)-2-(4,7-dimethyl-1-indenyl)methyl benzeneHCID 18471716—

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

4.12 ml (10.3 mmoles) of n-BuLi 2.5 M in hexane are added to a solution of 1.48 g of 4,7-dimethyl indene (XVIII) (10.3 mmoles; obtained as described above) in 55 ml of a mixture of THF-hexane 2/1. At the end of the addition, the mixture is left under stirring for 1 hour. It is then cooled to −70° C. and a solution of 2.3 g of the brominated compound having formula (XX) (7.37 mmoles) in THF/hexane are added dropwise. The mixture is left to rise to room temperature and is left to rest for 6 hours. It is then poured into water and is extracted with ethyl ether. The organic phase is washed until neutrality and dehydrated on sodium sulfate. The residue obtained by evaporation of the solvent is purified by silica gel chromatography eluating with petroleum ether. After evaporation of the eluant 2.0 g of the bis-indenyl ligand having formula (XXI) and indicated below, are obtained (72% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06211110B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-5126c223f2b14f7bab136e8816d4a689
Quellennotizuspto-grants-2001_04