Reacción #2021472

ord-00fdde93543d477180aa7410524e7584

Ecuación de reacción

O=C1OCCC1Br
α-bromo-γ-butyrolactone
C=C(C)C(=O)O
methacrylic acid
CC(=O)CC(C)C
methyl isobutyl ketone
C=C(C)C(=O)OC1CCOC1=O
α-methacryloyloxy-γ-butyrolactone
Rendimiento 85.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added
  2. 2
    Otroto form a solution
  3. 3
    FiltraciónAfter filtration
  4. 4
    Lavadothe organic layer was washed with 5% aqueous sodium hydrogen carbonate-solution
  5. 5
    Lavadowashed twice with water
  6. 6
    ConcentraciónThe organic layer was concentrated

Procedimiento

After charging 100 parts of α-bromo-γ-butyrolactone and 104.4 parts of methacrylic acid (2.0 times in mole based on α-bromo-γ-butyrolactone), a three times amount of methyl isobutyl ketone based on α-bromo-γ-butyrolactone was added thereto to form a solution. To this solution was added dropwise 183.6 parts of triethylamine (3.0 times in mole based on α-bromo-γ-butyrolactone). Then, the solution was stirred at room temperature for about 10 hours. After filtration, the organic layer was washed with 5% aqueous sodium hydrogen carbonate-solution and then washed twice with water. The organic layer was concentrated to give α-methacryloyloxy-γ-butyrolactone represented by the following formula in 85% yield:

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06383713B1uspto-grants-2002_05