反応 #5383

ord-e551bf9aea5c4c649c5667d952fb6c3a

反応方程式

CC(C)(c1ccc(OCC2CO2)cc1)c1ccc(OCC2CO2)cc1
diglycidyl ether of bisphenol A
CC(C)(c1ccc(OCC2CO2)cc1)c1ccc(OCC2CO2)cc1.Oc1cccc(O)c1
resorcinol diglycidyl ether of bisphenol A
Oc1cccc(O)c1
resorcinol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CCOCC.Oc1cccc(O)c1
resorcinol ether

溶媒

反応条件

温度
112°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他was prepared in a 3-liter reactor
  2. 2
    その他equipped with an agitator
  3. 3
    温度thermometer and reflux condenser
  4. 4
    workup.ADDITIONThe reactor was charged with about 330.3 g
  5. 5
    workup.ADDITIONThe stirred charge
  6. 6
    温度was heated
  7. 7
    温度The charge was refluxed for about one hour
  8. 8
    workup.ADDITIONamorphous silica was added

実験手順

A resorcinol/diglycidyl ether of bisphenol A addition product was prepared in a 3-liter reactor equipped with an agitator, thermometer and reflux condenser. The reactor was charged with about 330.3 g. resorcinol, 1500 ml. toluene and 3.0 g. triphenylphosphine. The stirred charge was heated to reflux at about 112° C. and about 654.0 g. diglycidyl ether of bisphenol A (Ciba-Geigy Araldite GY 6004) was added dropwise in about 2.5 hours. The charge was refluxed for about one hour, devolatilized at reduced pressure and about 36.0 g. amorphous silica was added to obtain a light tan resorcinol ether compound (RE4) having a 77° C. softening point, and having a 0.45 wt. % residual oxirane oxygen.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05244725uspto-grants-1993_09