Réaction #833531

ord-e3f4e262e9e142c089106b277f728fc4

Équation de réaction

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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07393624B2uspto-grants-2008_07