반응 #679305

ord-f24ece00b63f491da2628a67d68f1283

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타A monomer was prepared
  2. 2
    기타The jar was sealed
  3. 3
    기타placed in a 70° C.
  4. 4
    기타for 2 hours
  5. 5
    기타The resulting reaction mixture
  6. 6
    온도The reaction mixture was cooled
  7. 7
    기타The jar was then capped and refrigerated overnight
  8. 8
    기타The next day, the white crystals that had separated
  9. 9
    여과were filtered off
  10. 10
    기타dried
  11. 11
    기타to produce 26.9 g of NBMA

실험 절차

A monomer was prepared by adding 14.4 g 2-nitrobenzyl alcohol (Alfa Aesar, Ward Hill, Mass.), 14.6 g isocyanatoethyl methacrylate (Aldrich, Milwaukee, Wis.), and 1 drop of dibutyltin dilaurate (Alfa Aesar, Ward Hill, Mass.) to a 4-ounce jar. The jar was sealed and placed in a 70° C. oven for 2 hours. The resulting reaction mixture was analyzed by infrared spectroscopy (Nexus 670 FT-IR E.S.P.; Thermo Nicolet Corporation; Madison, Wis.) which showed no absorbance at 2250 cm−1, indicating substantially no remaining isocyanate functionality. The reaction mixture was cooled and 40 mL of toluene were added to it. The jar was then capped and refrigerated overnight. The next day, the white crystals that had separated were filtered off and dried to produce 26.9 g of NBMA. NMR and IR spectral analyses confirmed the structure of the product.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09238702B1uspto-grants-2016_01