Reacción #1909803

Ecuación de reacción

9-fluorenone-4-carbonyl chloride

bis[4-(2-hydroxyethoxy) phenyl]sulfone

triethylamine

→

fluorenone

Disolventes

tetrahydrofuran

tetrahydrofuran

Condiciones de reacción

Tratamiento posterior

1. 1
   Otroequipped with a reflux condenser and a mechanical stirrer
2. 2
   TemperaturaThe solution was refluxed for 6 hours
3. 3
   Filtraciónfiltered hot
4. 4
   Otroto remove triethylamine hydrochloride salt byproduct
5. 5
   Otrothe filtrate was evaporated to dryness
6. 6
   Otroto obtain the crude product
7. 7
   OtroThe crude product was recrystallized from tetrahydrofuran with activated charcoal
8. 8
   OtroThe product was dried at 60° C. in a vacuum oven for 6 hours

Procedimiento

A 10.0 g quantity of 9-fluorenone-4-carbonyl chloride (0.04 mole, obtained from Aldrich Chemicals Co, Milwaukee, Wis. 53201, USA) and 100 ml of tetrahydrofuran (obtained from Aldrich) were added to a 250 ml, 3-neck round bottom flask equipped with a reflux condenser and a mechanical stirrer. The solution was stirred for about ½ hour, then 6.97 g of bis[4-(2-hydroxyethoxy) phenyl]sulfone (0.02 mole, obtained from Aldrich) in 50 ml of tetrahydrofuran were added, followed by the addition of 4.17 g of triethylamine (0.04 mole, obtained from Aldrich). The solution was refluxed for 6 hours, filtered hot to remove triethylamine hydrochloride salt byproduct, and the filtrate was evaporated to dryness to obtain the crude product. The crude product was recrystallized from tetrahydrofuran with activated charcoal. The product was dried at 60° C. in a vacuum oven for 6 hours to yield a fifth dimeric fluorenone derivative, which was a yellow solid (9.3 g, 60% yield). A 1H-NMR (300 MHz) spectrum in CDCl3 yielded chemical shifts (ppm) of: 4.35–4.43 (t, 4H); 4.72–4.81 (t, 4H); 6.95–7.05 (m, 4H); 7.27–7.38 (m, 4H); 7.40–7.52 (dd, 2H); 7.66–7.74 (dd, 2H); 7.79–7.94 (m, 8H); 8.25–8.33 (d, 2H).

Fuente