Reacción #352902

ord-f1a8535af413410c83dc3b564b346c4e

Ecuación de reacción

C=C(C)C(=O)OCCN=C=O
isocyanatoethyl methacrylate
Oc1ccc2ccccc2c1-c1c(O)ccc2ccccc12
1,1'-bi-2-naphthol
NC1CCCCC1
cyclohexylamine
CCCCCCCCCCCC(=O)[O-].CCCCCCCCCCCC(=O)[O-].CCC[CH2][Sn+2][CH2]CCC
dibutyltin dilaurate
C=C(C)C(=O)OCCNC(=O)NC1CCCCC1
1-cyclohexyl-3-methacryloxyethyl urea

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroA 3-neck, 250-mL round bottom flask equipped with a reflux condenser
  2. 2
    workup.STIRRINGThe reaction mixture was kept stirred for an additional 30 minutes
  3. 3
    FiltraciónThe solution was filtered
  4. 4
    Otroevaporated to dryness
  5. 5
    Otroto recover the product

Procedimiento

A 3-neck, 250-mL round bottom flask equipped with a reflux condenser was charged with isocyanatoethyl methacrylate (7.79 g), 1,1'-bi-2-naphthol (1.3 mg) and 50 mL of methylene chloride. While stirring, cyclohexylamine (5.24 g) and dibutyltin dilaurate (52.3 mg) in 50 mL of methylene chloride were added over a 15 minute period. The reaction mixture was kept stirred for an additional 30 minutes. The solution was filtered and evaporated to dryness to recover the product. The product was characterized by H-NMR, 0.72-2.10 ppm (m, 1H), 1.90 ppm (s, 3H), 3.45 ppm (t, 2H), 3.50 ppm (hidden, 1H), 4.18 ppm (t, 2H), 5.12 ppm (s, 1H), 5.26 ppm (s, 1H), 5.52 ppm (s, 1H), 6.10 ppm (s, 1H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05648515uspto-grants-1997_07