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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1029066Erstellt: 26. Oktober 2026

1-Iodooctane → 2-Iodo-9,9-dioctylfluorene

https://huagongshe.com/reaction/1029066

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-IodooctaneHCID 12380—
Edukt2-Iodo-9H-fluoreneHCID 224094—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Iodo-9,9-dioctylfluoreneHCID 23072873—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

20 parts of 2-iodofluorene was dissolved in a mixed solution of 114 parts of dimethyl sulfoxide (DMSO) and 23 parts of tetrahydrofuran (THF), and the thus obtained mixture was then stirred at 25° C. for 10 minutes. Thereafter, while stirring, 8.7 parts of potassium-tert-butoxide was added to the mixture. Twenty minutes later, 19.2 parts of n-octyl iodide was added to the mixture, and further twenty minutes later, 8.7 parts of potassium-tert-butoxide was added thereto. Further, twenty minutes later, 19.2 parts of n-octyl iodide was added thereto, and the obtained mixture was then stirred at 25° C. for 2 hours. After completion of the stirring, THF was distilled away from the reaction solution, and it was then extracted with toluene-water. The toluene phase was dried over magnesium sulfate, and the toluene was then distilled away, thereby obtaining a brown tarry solid. This brown tarry solid was separated and purified by column chromatography (hexane-ethyl acetate) to obtain 30 parts of 9,9-di-n-octyl-2-iodofluorene in the form of a colorless crystal.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08735720B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-ba46631032444715a3a499b93bf72428
Quellennotizuspto-grants-2014_05