反应 #65055

ord-30a4a3242f2646b08954fcbe4f12329c

反应方程式

CC(=O)C1CC(C)OC1=O
3-acetyl-5-methyldihydro-2(3H)-furanone
[Na+].[OH-]
sodium hydroxide
O=CC1CCCCC1
cyclohexanecarboxaldehyde
CC1CC(=CC2CCCCC2)C(=O)O1
3-cyclohexylmethylene-5-methyldihydro-2(3H)-furanone
收率 97.8%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他for the reaction
  2. 2
    workup.ADDITIONadded
  3. 3
    workup.STIRRINGto stir for 10 minutes
  4. 4
    温度heated
  5. 5
    workup.ADDITIONwas added over a one-hour period
  6. 6
    温度The mixture was heated
  7. 7
    温度under reflux for an additional twelve hours
  8. 8
    温度cooled

实验过程

Example I was repeated using propionaldehyde diethyl acetal as the azeotroping solvent for the reaction. For the reaction 100 ml propionaldehyde diethyl acetal was charged to the reactor with 14.9 g (0.10 mole) 3-acetyl-5-methyldihydro-2(3H)-furanone. The mixture was stirred and 4 g (0.10 mole) powdered sodium hydroxide added. The mixture was allowed to stir for 10 minutes and then heated to reflux for 51/2 hours after which time 14.0 g (0.125 mole) cyclohexanecarboxaldehyde was added over a one-hour period. The mixture was heated under reflux for an additional twelve hours, cooled and worked up to recover 19 g crude 3-cyclohexylmethylene-5-methyldihydro-2(3H)-furanone (59% yield). The structure of the product was confirmed by proton and carbon nuclear magnetic resonance spectroscopy.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05416224uspto-grants-1995_05