O-Xylene → HCID 19808162, compound
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]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
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
- custombeing kept at 110° C
- waitThe whole was kept at 110° C. for half an hour
- customrose to 105° C
- customwas removed azeotropically at reduced pressure (200 mbar)
- customThe salt formed
- filtrationthe Dowex were filtered off
- washThe residue was washed twice with 20 ml ECH
- 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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