Reaktion #461739

ord-211bce0f83a84d9ca3ee5ed86965c952

Reaktionsgleichung

CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1
isophorone diisocyanate
C=C(C)c1cccc(C(C)(C)N=C=O)c1
m-isopropenyl-α,α-dimethylbenzyl isocyanate
C=C(C)C(=O)OC(C(F)(F)F)C(F)(F)F
hexafluoroisopropyl methacrylate
C=C(C)c1ccccc1
α-methyl styrene

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled in an ice-water bath
  2. 2
    workup.STIRRINGthe mixture is stirred for 2 hours at room temperature until all isocycanate
  3. 3
    workup.STIRRINGthe mixture is stirred for 2 more hours

Vorschrift

9.045 g (5.53 m equiv. amine) of an α,ω-di-propylamino-poly-(dimethyl siloxane) of MW 1636 (Shin Etsu Corp. No. X-22-161A) are placed in a 1 oz. jar; 4.56 g of hexafluoroisopropyl methacrylate (F6MA) are added and the mixture is stirred and cooled in an ice-water bath. 0.21 g (0.9546 m moles) of isophorone diisocyanate (IPDI) are added and the mixture is stirred for 2 hours at room temperature until all isocycanate has disappeared (by IR). Then 1.85 g (9.22 m moles) m-isopropenyl-α,α-dimethylbenzyl isocyanate (TMI) are added and the mixture is stirred for 2 more hours to yield a clear viscous liquid of a 70.90% solution of α-methyl styrene capped, chain extended poly(dimethyl siloxane) of MW 2426 (calculated) in F6MA.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05480946uspto-grants-1996_01