تفاعل #49633

ord-66573b26e9d24df49d64b3e512da4a5e

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05422038uspto-grants-1995_06