反应 #338694

ord-326ae3cc2a4e4786a8b162abd8b8c073

反应方程式

C=CCN1C(=O)C2CC=CCC2C1=O
N-allyl-4-cyclohexene-1,2-dicarboximide
NCP(=O)(O)O
aminomethylphosphonic acid
O.OO
hydrogen peroxide water
C=CCN1C(=O)C2CC3OC3CC2C1=O
4,5-epoxy-N-allylcyclohexane-1,2-dicarboximide

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他In a 50 mL three-necked flask equipped with stirrer
  2. 2
    温度The mixture was heated
  3. 3
    其他kept at 90° C.
  4. 4
    温度It was then cooled in an ice bath
  5. 5
    其他after removing the excess hydrogen peroxide
  6. 6
    萃取with 15 mL of saturated aqueous sodium thiosulfate, extraction
  7. 7
    干燥The obtained ethyl acetate solution was dried overnight over anhydrous sodium sulfate
  8. 8
    其他a rotary evaporator
  9. 9
    其他to remove the ethyl acetate solvent
  10. 10
    其他to obtain 3.21 g of a crude product of 4,5-epoxy-N-allylcyclohexane-1,2-dicarboximide
  11. 11
    其他purification

实验过程

In a 50 mL three-necked flask equipped with stirrer, dropping funnel and Dimroth condenser tube there were charged 5.15 g of N-allyl-4-cyclohexene-1,2-dicarboximide, 0.23 g of methyltrioctylammonium hydrogensulfate, 0.22 g of sodium tungstate dihydrate and 0.03 g of aminomethylphosphonic acid. The mixture was heated using an oil bath kept at 90° C., and after adding 4 ml of 30% hydrogen peroxide water dropwise over a period of 30 minutes through a dropping funnel, the mixture was aged for 4 hours. It was then cooled in an ice bath, and after removing the excess hydrogen peroxide with 15 mL of saturated aqueous sodium thiosulfate, extraction was performed 5 times with 10 mL of ethyl acetate. The obtained ethyl acetate solution was dried overnight over anhydrous sodium sulfate, a rotary evaporator was used to remove the ethyl acetate solvent to obtain 3.21 g of a crude product of 4,5-epoxy-N-allylcyclohexane-1,2-dicarboximide, and then purification was performed by chromatography with a column packed with 25% hydrated silica gel. Structural isomers of 4,5-epoxy-N-allylcyclohexane-1,2-dicarboximide exist due to the epoxy group, and of these there were obtained 0.72 g of 4,5-epoxy-N-allylcyclohexane-1,2-dicarboximide 1 and 0.56 g of 4,5-epoxy-N-allylcyclohexane-1,2-dicarboximide 2. An AL-400 nuclear magnetic resonance apparatus by JEOL Corp. was used to measure the 1H-NMR and 13C-NMR spectra of the 4,5-epoxy-N-allylcyclohexane-1,2-dicarboximide 1 in a heavy chloroform solvent, thus allowing confirmation of the structure. The 1H-NMR and 13C-NMR spectra of the 4,5-epoxy-N-allylcyclohexane-1,2-dicarboximide 1 are shown in FIGS. 1 and 2, respectively, and the 1H-NMR integral values of the 4,5-epoxy-N-allylcyclohexane-1,2-dicarboximide 1 are shown in Table 1 below.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07863461B2uspto-grants-2011_01