Reaktion #701146

ord-898bf593abef4d92a784e63464e7e1ed

Reaktionsgleichung

Oc1ccc(O)cc1
hydroquinone
CC(C(=O)OC(=O)C(C)S(=O)(=O)O)S(=O)(=O)O
sulfopropionic anhydride
C=C(C)C(=O)OCC(C)O
2-hydroxypropyl methacrylate
COC
monomethyl ether
→
C=C(C)C(=O)OC(C)(C)OC(=O)C(C)S(=O)(=O)O
METHACRYLOXYISOPROPYL SULFOPROPIONATE

Edukte

Oc1ccc(O)cc1
hydroquinone
CC(C(=O)OC(=O)C(C)S(=O)(=O)O)S(=O)(=O)O
sulfopropionic anhydride
C=C(C)C(=O)OCC(C)O
2-hydroxypropyl methacrylate
COC
monomethyl ether

Reagenzien

Keine

Lösungsmittel

Cc1ccccc1
toluene

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeTo a reaction vessel fitted with an air-bleed tube
  2. 2
    Sonstigesparged
  3. 3
    Sonstigewith dry air as in 1) above and
  4. 4
    Temperaturheated
  5. 5
    workup.ADDITIONAfter 0.5 hour at 60° C. a solution containing 29% by weight of methacryloxyisopropyl sulfopropionate
  6. 6
    Sonstigeis obtained

Vorschrift

To a reaction vessel fitted with an air-bleed tube, thermometer, stirrer, and condenser there are charged sulfopropionic anhydride (29.1 g.), 2-hydroxypropyl methacrylate (29.1 g.), the monomethyl ether of hydroquinone (0.1 g.) and toluene (60 g.). The mixture is stirred, sparged with dry air as in 1) above and heated. After 0.5 hour at 60° C. a solution containing 29% by weight of methacryloxyisopropyl sulfopropionate is obtained.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04143020uspto-grants-1979_03