HRID2226646

反应详情

EQUATION

反应方程式

HRID 2226646 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A mixture of 17.82 g (92.8 mmoles) of 6,10-dimethyl-3,5,9-undecatrien-2-one ("pseudoionone", prepared from citral and acetone as described by A. Russell, et al., Organic Syntheses, Collective Volume 3, pages 747-750) and 1.0 g of 5% palladium on activated carbon in 50 mL of absolute ethyl alcohol was shaken vigorously under a hydrogen atmosphere (approximately 2-3 atm. pressure) for 30 minutes. After removal of the catalyst by filtration through a small pad of Hyflo Super-Cel® filtering aid, the filtrate was diluted with 150 mL of hexane. The organic layer was subsequently washed with water (2×400 mL), then dried over anhydrous magnesium sulfate, and re-filtered. Removal of the hexane by evaporation at reduced pressure, followed by distillation, afforded 15.95 g (87% yield) of 6,10-dimethyl-2-undecanone: boiling point 68°-72° C. at 0.15 mm. A previous synthesis of the latter ketone has been reported by F. G. Fischer, et al., Ann., 475, 183 (1929).

WORKUP

后处理

  1. customAfter removal of the catalyst
  2. filtrationby filtration through a small pad of Hyflo Super-Cel®
  3. filtrationfiltering aid
  4. additionthe filtrate was diluted with 150 mL of hexane
  5. washThe organic layer was subsequently washed with water (2×400 mL)
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationre-filtered
  8. customRemoval of the hexane
  9. customby evaporation at reduced pressure
  10. distillationfollowed by distillation