Epichlorohydrin → Diglycidyl ether

HRID 1742893Notes

Reaction equation

HRID 1742893 reaction equation
C(O)[CH2:2][CH2:3][CH2:4][OH:5].[CH2:7]([CH:9]1[O:11][CH2:10]1)Cl.[OH-:12].[Na+]>>[CH2:7]([O:5][CH2:4][CH:3]1[O:12][CH2:2]1)[CH:9]1[O:11][CH2:10]1

Participants

4

Conditions

Temperature
100 °C

Procedure

In a 750 ml sulfonation flask equipped with thermometer, reflux condenser, N2 inlet and metering device, 90.12 g (1.0 mol) of 1,4-butanediol are added to catalyst B and the reaction mixture is heated to 100° C. With efficient stirring, 160.7 ml (2.05 mol) of epichlorohydrin are added over 1 h and the mixture is allowed to react for 1 h. Afterwards the reaction mixture is cooled to 50° C. and to the solution are added 16 g (0.2 mol) of a 50% aqueous solution of NaOH over 5 min. Then 76 g (1.9 mol) of pulverised NaOH are added by increments over 45 min and the suspension is stirred for 30 min. The reaction mixture is filtered, washed with 100 ml of toluene and the phases are separated. The organic phase is dried over MgSO4, filtered and the filtrate is freed from solvent on a rotary evaporator (bath temperature 70° C.), giving 199.0 g (98% of theory) of colourless diglycidyl ether of 1,4-butanediol having the following properties: epoxy value: 8.64 eq/kg (87% of theory); total chlorine content: 3.4%; concentration of hydrolisable chlorine: 620 ppm.

Workup

  1. customIn a 750 ml sulfonation flask equipped with thermometer
  2. temperaturereflux condenser, N2 inlet
  3. customto react for 1 h
  4. temperatureAfterwards the reaction mixture is cooled to 50° C. and to the solution
  5. filtrationThe reaction mixture is filtered
  6. washwashed with 100 ml of toluene
  7. customthe phases are separated
  8. dry with materialThe organic phase is dried over MgSO4
  9. filtrationfiltered
  10. customthe filtrate is freed from solvent on a rotary evaporator (bath temperature 70° C.)

Sources & evidence

ORD record
ord-8ce8f4994d4045d18f4441484483def7
Source dataset
uspto-grants-1994_08
Patent number
US05342903

Reaction notes

Loading…