Réaction #550992

ord-fb76d87f9db040eb8df132a044ce127d

Équation de réaction

CCCCC[N+](CCCCC)(CCCCC)CCCCC.N#C[O-]
tetraamylammonium cyanate
C1CCOC1
tetrahydrofurane
O=C=O
CO2
O=C=NCCCCCCN=C=O
hexamethylene diisocyanate
CCCCC[N+](CCCCC)(CCCCC)CCCCC.CCCCC[N+](CCCCC)(CCCCC)CCCCC.O=C([O-])C1=NNOC=C1.O=C([O-])C1=NNOC=C1
tetraamylammonium bis-oxadiazinate
Rendement 94.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreAfter 10 minutes of reaction
  2. 2
    Autrethe solvent is evaporated
  3. 3
    Lavagethe obtained solid is washed with carbon tetrachloride

Mode opératoire

34.6 g of tetraamylammonium cyanate (0.1 mole) and 250 ml of tetrahydrofurane are introduced into the reactor described in example 1. The solution is maintained saturated with CO2 at the atmospheric pressure. 8.4 g of hexamethylene diisocyanate (0.05 mole) are progressively added during 5 minutes. After 10 minutes of reaction, the solvent is evaporated and the obtained solid is washed with carbon tetrachloride. 44 g (yield: 94%) of tetraamylammonium bis-oxadiazinate of the following formula are obtained: ##STR17## this compound having a structure corresponding to that of formula (I).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04544743uspto-grants-1985_10