反应 #5340

ord-167fda6db42f40c2b04d4c02c0deb86d

反应方程式

c1ccc(OCC2CO2)cc1
phenyl glycidyl ether
C1CO1
oxirane
Cc1ccc(S(=O)(=O)O)cc1.O
p-toluenesulfonic acid monohydrate
c1ccc2c(c1)Nc1ccccc1S2
phenothiazine
OCC(O)COc1ccccc1
3-Phenoxy-1,2-propanediol

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度at reflux for 6.0 hours
  2. 2
    温度Upon cooling
  3. 3
    workup.ADDITIONthe reactor was charged with 186.0 g
  4. 4
    温度The mixture was again heated
  5. 5
    温度at reflux
  6. 6
    萃取The product was extracted with ether
  7. 7
    其他purified
  8. 8
    洗涤by washing
  9. 9
    其他at 25° C.

实验过程

A solution of 150.2 g. phenyl glycidyl ether (1.0 eq.), 200.0 g. AOnPA (1.15 eq., of Example 1), 200.0 g. toluene, 4.0 g. tetrapropylammonium bromide (0.015 eq.), and 1.0 g. phenothiazine was heated at reflux for 6.0 hours. Conversion, measured by residual oxirane titer, was ca. 93%. Upon cooling, the reactor was charged with 186.0 g. of the AOnPA (1.07 eq.), 150.0 g. toluene, and 10.0 g. p-toluenesulfonic acid monohydrate (0.05 eq.). The mixture was again heated at reflux. After 6.0 hrs., conversion was 90%. The product was extracted with ether and purified by washing. It had an acrylate titer of 3.8 meq./g. (theory: 4.17 meq./g.) and Brookfield viscosity of 230 centipoise at 25° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05243069uspto-grants-1993_09