Reaktion #1365711

ord-3901f3841ab847a79d34516e6d4156e3

Reaktionsgleichung

C[Si](C)(C)C(Cl)[Si](C)(C)C
Bis(trimethylsilyl)chloromethane
C=CC(=O)[O-].[Na+]
sodium acrylate
c1ccc2c(c1)Nc1ccccc1S2
phenothiazine
C=CC(=O)OC([Si](C)(C)C)[Si](C)(C)C
desired product
C=CC(=O)OC([Si](C)(C)C)[Si](C)(C)C
Bis(trimethylsilyl)methylacrylate

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeequipped with a condenser, mechanical stirrer and a nitrogen inlet
  2. 2
    Temperaturheated
  3. 3
    Temperaturto reflux
  4. 4
    Filtrationfiltered
  5. 5
    Sonstigeto remove the solids
  6. 6
    SonstigeThe solvents were removed under reduced pressure
  7. 7
    workup.DISTILLATIONFractional distillation of the residue under reduced pressure

Vorschrift

Bis(trimethylsilyl)chloromethane (Aldrich) 39 g, 0.2 mole), sodium acrylate (28 g, 0.3 mole), Adogen 464 (Aldrich) (6.96 g), and phenothiazine (0.10 grams) were placed in a round bottom flask equipped with a condenser, mechanical stirrer and a nitrogen inlet. The flask was charged with 100 ml of butyronitrile and heated to reflux while stirring. After 6 hours, the mixture was diluted with 150 ml hexanes and filtered to remove the solids. The solvents were removed under reduced pressure. Fractional distillation of the residue under reduced pressure gave 35.5 grams 975%) of the desired product at 45-58° C. at 0.5 mm pressure.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06444408B1uspto-grants-2002_09