Reacción #52247

ord-744b6f7830e74138ba8d3a0fa822c2b4

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otropurged with nitrogen
  2. 2
    workup.ADDITIONOne drop of dibutyl tin dilaurate was added to the solution
  3. 3
    workup.STIRRINGto stir overnight
  4. 4
    Otroa white precipitate was obtained
  5. 5
    Otroafter solvent removal m.p. 105-112° C. (40.5 g, 100%)

Procedimiento

Hydroxy ethylmaleimide (10 g, 0.141 mol) was dissolved in acetone and purged with nitrogen while stirring in an ice bath. One drop of dibutyl tin dilaurate was added to the solution. The isophorone diisocyanate (30.5 g, 0.141 mol) was added dropwise over 2-3 hours. The solution was allowed to stir overnight and a white precipitate was obtained after solvent removal m.p. 105-112° C. (40.5 g, 100%). 1H-NMR (D6-DMSO, δ, ppm): 3.63-3.58 (2H, —NCH2—), 4.08-4.03 (2H, —CH2O—, t), 7.03 (2H, —CH═CH—, s). 13C-NMR (D6-DMSO, δ, ppm): 134.5 (2C, —CH═CH—), 154.9 (2C, NHC═O), (170.7 (2C, —NC═O).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06855745B2uspto-grants-2005_02