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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 720018Erstellt: 26. Oktober 2026

Dimethylformamide → 2-Bromo-9,9-dimethoxyethylfluorene

https://huagongshe.com/reaction/720018

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt2-Bromo-9H-fluoreneHCID 14336—
Edukt2-Bromoethyl methyl etherHCID 80972—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelWaterHCID 962—
Produkt2-Bromo-9,9-dimethoxyethylfluoreneHCID 69587088—

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

To a solution of 2-bromofluorene (2.0 g, 8.2 mmol) in dimethylformamide (dry, 30 ml) was added potassium t-butoxide (2.74 g, 24.4 mmol), giving a deep orange in color. The mixture was stirred at 45° C. for 20 min and added 2-bromoethylmethyl ether (3.5 g, 2.5 mmol) dropwise. Stirring was continued at the same temperature for overnight to give an orange solution. Another portion of 2-bromoethylmethyl ether (1.4 g, 1.0 mmol) was added and the mixture stirred at 80° C. for 4 h. It was diluted with water (100 ml). The products extracted with ethylacetate (20 ml) and washed with water. Organic layer was dried over magnesium sulfate and concentrated in vacuuo to afford the crude product. It was purified by preparative thin layer chromatography (silica gel, Rf=0.3 using hexane-EtOAc/3:2 as eluent) to give 2-bromo-9,9-dimethoxyethylfluorene (1.5 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07132572B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-dc989689314d4eefbdcd9bd4ab551516
Quellennotizuspto-grants-2006_11