Reacción #833531

ord-e3f4e262e9e142c089106b277f728fc4

Ecuación de reacción

CC(C)(O)CCCl
1-chloromethyl-2-methyl-2-propanol
C=C(C)C(=O)[O-].[Na+]
sodium methacrylate
c1ccc2c(c1)Nc1ccccc1S2
phenothiazine
C=C(C)C(=O)OCC(C)(C)O
2-hydroxy-2,2-dimethylethyl methacrylate

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas heated
  2. 2
    Temperaturato reflux under nitrogen in a three-necked round bottomed flask
  3. 3
    Otroequipped with a condenser and a mechanical stirrer
  4. 4
    Filtraciónfiltered through celite
  5. 5
    OtroThe solvents were removed under aspirator vacuum (40-80° C.)
  6. 6
    workup.DISTILLATIONThe residue was distilled under high vacuum
  7. 7
    OtroThe 22.50 grams of the product was collected between 72-80° C. at 2 mm pressure as a clear liquid

Procedimiento

A mixture of 1-chloromethyl-2-methyl-2-propanol (21.80 g, 0.20 mole), sodium methacrylate (32.40 g, 0.30 mole), Adogen 464 (7.00 g, 0.015 mole) (phase transfer catalyst purchased from Aldrich Chemical Co.), and phenothiazine (60 mg) in butyronitrile (200 ml) was heated to reflux under nitrogen in a three-necked round bottomed flask equipped with a condenser and a mechanical stirrer. After cooling the contents to room temperature, the mixture was diluted with hexane (200 ml) and filtered through celite. The solvents were removed under aspirator vacuum (40-80° C.). The residue was distilled under high vacuum. The 22.50 grams of the product was collected between 72-80° C. at 2 mm pressure as a clear liquid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07393624B2uspto-grants-2008_07