Reaktion #2775

ord-57f6a6d0eb6f4093927d8288234b69ac

Reaktionsgleichung

Oc1ccc(O)cc1
hydroquinone
C=C(C)C(=O)Cl
methacryloyl chloride
C=C(C)C(=O)O.Oc1ccc(O)cc1
hydroquinone monomethacrylate

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturmaintained at 0° to 5° C
  2. 2
    workup.STIRRINGAfter stirring for one more hour at room temperature
  3. 3
    Sonstigethe acetone was evaporated
  4. 4
    workup.ADDITIONWater was then added
  5. 5
    Extraktionwith ether extraction
  6. 6
    WaschenAfter washing this ether layer with a 5% aqueous solution of sodium hydrogencarbonate
  7. 7
    Waschenthe solution was then washed with water
  8. 8
    Trocknendried (anhydrous sodium carbonate)
  9. 9
    SonstigeThe ether was then evaporated out, with a white solid being
  10. 10
    Sonstigeobtained
  11. 11
    SonstigeThis was recrystallized from water

Vorschrift

350 g of hydroquinone was dissolved in 2.5 kg of acetone and 500 ml of pyridine. After cooling to 0° C., 313.5 g of methacryloyl chloride was added dropwise, with the reaction temperature maintained at 0° to 5° C. Stirring was then carried out for 3 hours at the same temperature. After stirring for one more hour at room temperature, the acetone was evaporated. Water was then added, and hydrochloric acid was used to adjust the solution to an acidic pH (pH 4), with ether extraction then performed. After washing this ether layer with a 5% aqueous solution of sodium hydrogencarbonate, the solution was then washed with water and dried (anhydrous sodium carbonate). The ether was then evaporated out, with a white solid being obtained. This was recrystallized from water, to obtain 420 g of colorless, needle crystals of hydroquinone monomethacrylate having a melting point of 120.5° to 121.5° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05731127uspto-grants-1998_03