HRID1578328

反应详情

EQUATION

反应方程式

HRID 1578328 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Sodiomethylacetoacetate was prepared by adding an excess of methylacetoacetate (74.3 g, 0.64 mole) to a solution of sodium ethoxide (31.3 g, 0.46 mole) in 150 mls. absolute ethanol at 25°. The reaction mixture was cooled to 0° and then the crude chloride prepared above was added dropwise over a 25-minute period and stirring was continued at 0° for an additional 3 hours. After this period, the temperature was allowed to rise to ambient over a 40-minute period. A portion of the ethanol (78.0 g) was distilled at this point by stirring the reaction mixture at 60°-65° for 2 hours under a slight vacuum. After cooling to 30°, 550 mls. of 10% aqueous NaOH was added over a 15-minute period and the reaction mixture was stirred at 70° for 4 hours. After settling, the layers were separated and the aqueous layer was saturated with NaCl and extracted with three 200-ml. portions of pentane. The combined oils were washed once with 1 liter H2O and once with 1 liter saturated NaCl to yield, after solvent removal, 139.2 g of crude 6,10,14-trimethylpentadeca-5,9-dien-2-one. Gas chromotographic analysis indicated 53.2% purity which represents an estimated theory yield from 10,11-dihydrofarnesene of 78.8%.

WORKUP

后处理

  1. customat 25°
  2. temperatureThe reaction mixture was cooled to 0°
  3. additionabove was added dropwise over a 25-minute period
  4. waitAfter this period
  5. waitto ambient over a 40-minute period
  6. distillationA portion of the ethanol (78.0 g) was distilled at this point
  7. stirringby stirring the reaction mixture at 60°-65° for 2 hours under a slight vacuum
  8. temperatureAfter cooling to 30°
  9. additionof 10% aqueous NaOH was added over a 15-minute period
  10. stirringthe reaction mixture was stirred at 70° for 4 hours
  11. customthe layers were separated
  12. extractionextracted with three 200-ml
  13. washThe combined oils were washed once with 1 liter H2O and once with 1 liter saturated NaCl
  14. customto yield
  15. customafter solvent removal, 139.2 g of crude 6,10,14-trimethylpentadeca-5,9-dien-2-one
  16. customyield from 10,11-dihydrofarnesene of 78.8%