Reaktion #11277

Reaktionsgleichung

2-bromofluorene

DMSO

NaOH

n-octylbromide

→

2-bromo-9,9-dioctylfluorene

Ausbeute 155.4%

Lösungsmittel

water ether

hexane

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGStirring
2. 2
   workup.WAITwas continued for 2 hours
3. 3
   workup.ADDITIONTo the reaction mixture was added
4. 4
   Sonstigethe organic layer separated
5. 5
   Waschenwas washed successively with brine
6. 6
   TrocknenDrying over magnesium sulfate and evaporation of the solvent
7. 7
   Sonstigegave an oil
8. 8
   SonstigePurification by column chromatography (silica gel

Vorschrift

A 3L flask fitted with a mechanical stirrer was charged with 2-bromofluorene (45 g, 183.6 mmole) and 150 mL DMSO. Under a N2 atmosphere was added 80 mL of a 50% aqueous NaOH solution and 2.72 g of benzyltriethylammonium chloride (2.72 g, 11.98 mmole). This was stirred for 2 h at RT. With vigorous mechanical stirring, n-octylbromide (84.96 g, 440 mmole) was added via a dropping funnel (exotherm). Stirring was continued for 2 hours. To the reaction mixture was added 500 mL of a 1:1 mixture of water/ether, and the organic layer separated and was washed successively with brine and then water. Drying over magnesium sulfate and evaporation of the solvent gave an oil. Purification by column chromatography (silica gel; hexane as the mobile phase) gave 67 g (78% yield) of 2-bromo-9,9-dioctylfluorene as a pale oil.

Quelle