Reacción #49633

Ecuación de reacción

ethyl acetoacetate

sodium

2-bromomethylnaphthalene

→

2-(2-ethoxycarbonyl-3-oxobutyl)naphthalene

Rendimiento 114.1%

Disolventes

ethanol

ethanol

ethanol

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroIn a four-necked flask equipped with a thermometer
2. 2
   Otroto form a solution
3. 3
   workup.ADDITIONAfter completion of the addition
4. 4
   Otrowas brought up to 65° C.
5. 5
   workup.DISTILLATIONwas distilled off under reduced pressure
6. 6
   Otrothe residue obtained
7. 7
   Extracciónwas extracted by addition of 1500 ml of toluene
8. 8
   Otrothe organic layer was separated
9. 9
   LavadoThe organic layer was washed with 10% hydrochloric acid, water, 5% aqueous sodium bicarbonate solution and water in said order
10. 10
    Concentraciónconcentrated under reduced pressure

Procedimiento

In a four-necked flask equipped with a thermometer, dropping funnel and stirrer were placed 179 g (1.375 moles) of ethyl acetoacetate and 500 ml of ethanol, and then 31.5 g (1.375 moles) of sodium was added in portions thereto to form a solution. Then, a solution of 276.4 g (1.25 moles) of 2-bromomethylnaphthalene in 1000 ml of ethanol was added dropwise to the above solution at room temperature over a period of 2 hours. After completion of the addition, the resulting mixture was brought up to 65° C. and stirred at the same temperature for 6 hours. After completion of the reaction ethanol was distilled off under reduced pressure, the residue obtained was extracted by addition of 1500 ml of toluene, and the organic layer was separated. The organic layer was washed with 10% hydrochloric acid, water, 5% aqueous sodium bicarbonate solution and water in said order and then concentrated under reduced pressure to obtain 385.4 g of 2-(2-ethoxycarbonyl-3-oxobutyl)naphthalene as a crude product.

Fuente