O-Xylene → HCID 19808162, compound

HRID 1681053Notes

Reaction equation

HRID 1681053 reaction equation
[OH-].[Na+].[OH:3][CH2:4][C:5]([CH3:10])([CH3:9])[C:6]([OH:8])=[O:7].C1(C)C(C)=CC=CC=1.[CH2:19]([CH:21]1[O:23][CH2:22]1)Cl>O>[CH2:19]([O:7][C:6](=[O:8])[C:5]([CH3:10])([CH3:9])[CH2:4][OH:3])[CH:21]1[O:23][CH2:22]1

Participants

6

Conditions

Temperature
50 °C

Procedure

96 parts by wt. 50% sodium hydroxide solution (in water) were added dropwise in 1 hour to 118 parts by wt. (1 1 mole) hydroxypivalic acid and 200 ml xylene, the temperature of the reaction mixture being kept at 110° C. The whole was kept at 110° C. for half an hour. After cooling to 50° C., 276 parts by wt. (3 mole) epichlorohydrin and 50 g Dowex were added to the reaction mixture. The temperature of the reaction mixture rose to 105° C. At this temperature the mixture was afterreacted for 1 hour. After cooling to 50° C. the water was removed azeotropically at reduced pressure (200 mbar). The salt formed and the Dowex were filtered off. The residue was washed twice with 20 ml ECH. The entire organic phase (ECH+xylene) was removed by means of rotary film evaporation. Thus 160 parts by wt. hydroxypivalic glycidyl ester were obtained in the form of a light yellow liquid with an epoxide content of 5.6 meq/g and a hydroxy content of 310 mg KOH/g.

Workup

  1. custombeing kept at 110° C
  2. waitThe whole was kept at 110° C. for half an hour
  3. customrose to 105° C
  4. customwas removed azeotropically at reduced pressure (200 mbar)
  5. customThe salt formed
  6. filtrationthe Dowex were filtered off
  7. washThe residue was washed twice with 20 ml ECH
  8. customThe entire organic phase (ECH+xylene) was removed by means of rotary film evaporation

Sources & evidence

ORD record
ord-a552869613ae4140a269536fbec37c5d
Source dataset
uspto-grants-1992_12
Patent number
US05168110

Reaction notes

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