Reacción #2460287

Ecuación de reacción

1,3-dicyclohexylcarbodiimide

2-butynoic acid

9-fluorenemethanol

dimethylamino-pyridine-p-toluenesulfonic acid salt

→

9-fluorenylmethyl 2-butynoate

Rendimiento 55.3%

Disolventes

dichloromethane

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroFirst, 9-fluorenylmethyl 2-butynoate was prepared
2. 2
   Temperaturathe reaction mixture was warmed to ambient and
3. 3
   FiltraciónThe urea by product was filtered
4. 4
   Lavadothe filtrate was washed successively with 10% aqueous HCl, 10% aqueous NaHCO3, water, and brine
5. 5
   SecadoThe solution was dried (Na2SO4)
6. 6
   Concentraciónconcentrated
7. 7
   OtroThe product was purified by column chromatography

Procedimiento

First, 9-fluorenylmethyl 2-butynoate was prepared. A mixture of 2-butynoic acid (11.6 g, 138 mmol), 9-fluorenemethanol (35.2 g, 179 mmol), dimethylamino-pyridine-p-toluenesulfonic acid salt (16.3 g, 55 mmol), and anhydrous dichloromethane (210 mL) was cooled to 0° C. under nitrogen, and 1,3-dicyclohexylcarbodiimide (34.2 g, 166 mmol) was added. After 15 min, the reaction mixture was warmed to ambient and stirred for 12 h. The urea by product was filtered, and the filtrate was washed successively with 10% aqueous HCl, 10% aqueous NaHCO3, water, and brine. The solution was dried (Na2SO4) and concentrated to deposit a yellow oil. The product was purified by column chromatography to provide 20.0 g (54% of theory) of 9-fluorenylmethyl 2-butynoate as a yellow-green solid. 1H NMR (CDCl3): δ 1.98 (s, 3H), 4.20 (m, 1H), 4.45 (d, 2H), 7.32 (m, 4H), 7.60 (d, 2H), 7.70 (d, 2H).

Fuente