Reacción #11277

Ecuación de reacción

2-bromofluorene

DMSO

NaOH

n-octylbromide

→

2-bromo-9,9-dioctylfluorene

Rendimiento 155.4%

Disolventes

water ether

hexane

Condiciones de reacción

Tratamiento posterior

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

Procedimiento

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.

Fuente