Reacción #95198

ord-5ff3b8f09cfb48e092f5800cf9912f1a

Ecuación de reacción

O
water
CC(=O)C(C)=NO
butanedione monoxime
CCN(CC)CC
triethylamine
C=C(C)C(=O)Cl
methacryloyl chloride
C=C(C)C(=O)O.CC(=O)C(C)=NO
OBM
C=C(C)C(=O)O.CC(=O)C(C)=NO
3-oximino-2-butanone methacrylate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe monomer 3-oximino-2-butanone methacrylate (OBM) was prepared
  2. 2
    Temperaturaby cooling to a temperature of 0 degree C
  3. 3
    Otrowas continued under nitrogen at 0 degree
  4. 4
    workup.ADDITIONfor 3 hours after the addition
  5. 5
    FiltraciónThe resulting mixture was filtered
  6. 6
    Otroto remove the solid residues
  7. 7
    Otrothe liquid obtained
  8. 8
    Otrowas transferred to a separatory funnel
  9. 9
    workup.STIRRINGthe liquid was agitated
  10. 10
    OtroThe water and ether phases were separated
  11. 11
    Secadothe ether phase was dried over magnesium sulfate for 1 hour
  12. 12
    OtroThe magnesium sulfate was removed by filtration
  13. 13
    Otrothe ether solution was evaporated to dryness on a rotary evaporator
  14. 14
    OtroThe resulting solid was recrystallized from cyclohexane

Procedimiento

The monomer 3-oximino-2-butanone methacrylate (OBM) was prepared. This preparation began by cooling to a temperature of 0 degree C. with an ice water bath, a solution of butanedione monoxime (54.5 g) and triethylamine (120 ml) in ether (1000 ml). Approximately 56 ml of methacryloyl chloride in 250 ml of ether was added dropwise under a nitrogen atmosphere over the course of 1 hour. The solution was stirred during this addition and the stirring was continued under nitrogen at 0 degree C. for 3 hours after the addition was completed. The resulting mixture was filtered to remove the solid residues. The solid residues were discarded, and the liquid obtained was transferred to a separatory funnel. Approximately 300 ml of water was added to the separatory funnel and the liquid was agitated. The water and ether phases were separated, the water phase was discarded, and the ether phase was dried over magnesium sulfate for 1 hour. The magnesium sulfate was removed by filtration and the ether solution was evaporated to dryness on a rotary evaporator using water aspirator vacuum. The resulting solid was recrystallized from cyclohexane to yield 45 g of OBM. (The material obtained melted between 38.5 and 39 degrees C.)

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04343889uspto-grants-1982_08