반응 #49633

ord-66573b26e9d24df49d64b3e512da4a5e

반응 방정식

CCOC(=O)CC(C)=O
ethyl acetoacetate
[Na]
sodium
BrCc1ccc2ccccc2c1
2-bromomethylnaphthalene
CCOC(=O)C(Cc1ccc2ccccc2c1)C(C)=O
2-(2-ethoxycarbonyl-3-oxobutyl)naphthalene
수율 114.1%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05422038uspto-grants-1995_06