p-Divinylbenzene → 2-(4-Ethenylphenyl)oxirane

HRID 845192

Reaction equation

HRID 845192 reaction equation
[CH:1]([C:3]1[CH:8]=[CH:7][C:6]([CH:9]=[CH2:10])=[CH:5][CH:4]=1)=[CH2:2].C(=O)([O-])[OH:12].[Na+].ClC1C=CC=C(C(OO)=O)C=1>C1(C)C=CC=CC=1>[CH:1]([C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[O:12][CH2:10]2)=[CH:5][CH:4]=1)=[CH2:2]

Participants

5

Procedure

Into a 1-liter reactor provided with a stirrer, and a thermometer, were added 25 g of p-divinylbenzene, 40 g of sodium hydrogencarbonate, and 400 ml of toluene. To the mixture, while being kept at 5° C. and stirred, was added dropwise a solution of 100 g (40% by weight) of m-chloroperbenzoic acid in toluene. The resulting mixture was stirred at 5° C. for 10 hours. After completion of the reaction, the reaction mixture was washed with aqueous sodium hydrogencarbonate solution, and dried over anhydrous magnesium sulfate. The mixture was filtered from the drying agent, then stripped of the toluene under reduced pressure, and purified by distillation to yield 65 g of 4-vinylstyrene oxide (1 Torr., 74° C.). In a similar manner, 3-vinylstyrene oxide was obtained from m-divinylbenzene.

Workup

  1. customInto a 1-liter reactor provided with a stirrer
  2. customwhile being kept at 5° C.
  3. stirringThe resulting mixture was stirred at 5° C. for 10 hours
  4. customAfter completion of the reaction
  5. washthe reaction mixture was washed with aqueous sodium hydrogencarbonate solution
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationThe mixture was filtered from the drying agent
  8. distillationpurified by distillation

Sources & evidence

ORD record
ord-bfd2dc5d57204b9da1f2586b838bee5a
Source dataset
uspto-grants-1988_07
Patent number
US04756989

Linked notes

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