Reacción #1166470

ord-7d9c2e6e85e0420ca204d7764a901ce8

Ecuación de reacción

NCC(O)CO
3-amino-1,2-propanediol
O=C1OC(=O)C2CCCCC12
hexahydrophthalic anhydride
C=CC(=O)OCC(CN1C(=O)C2CCCCC2C1=O)OC(=O)C=C
N-(2,3-dihydroxypropyl)hexahydrophthalimide
Rendimiento 109.7%
C=CC(=O)OCC(CN1C(=O)C2CCCCC2C1=O)OC(=O)C=C
N-(2,3-Di(acryloyloxy)propyl)hexahydrophthalimide
Rendimiento 109.7%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroA 500-ml, two necked flask was equipped with a magnetic stirring bar
  2. 2
    Temperaturaheating mantle and condenser
  3. 3
    Temperaturawas refluxed for 12 hours
  4. 4
    OtroThe ethanol was removed by a rotoevaporator

Procedimiento

A 500-ml, two necked flask was equipped with a magnetic stirring bar, heating mantle and condenser. The flask was charged with 46 g of 3-amino-1,2-propanediol (0.50 mol.) and 300 ml of ethanol. Next, 77 g of hexahydrophthalic anhydride (0.50 mol.) was slowly added to the flask after which the reaction was refluxed for 12 hours. The imide formation was confirmed by IR. The ethanol was removed by a rotoevaporator to yield 92 g (81%) of the N-(2,3-dihydroxypropyl)hexahydrophthalimide.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05580647uspto-grants-1996_12