Reaktion #417779

ord-e97171a3f19846d1bd33566ebb6b07ca

Reaktionsgleichung

C=CCN
allylamine
CCO[SiH](OCC)OCC
triethoxy silane
CCO[SiH](OCC)OCC
triethoxysilane
CCO[Si](CCCN)(OCC)OCC
gamma-aminopropyl triethoxy silane
C=CCN
allylamine
CCO[Si](CC(C)N)(OCC)OCC
beta-aminopropyl triethoxy silane

Lösungsmittel

Reaktionsbedingungen

Temperatur
110°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA three-neck flask equipped with a reflux condenser
  2. 2
    Temperaturheated on an oil bath
  3. 3
    SonstigeAbout 1 hour after the beginning of the reaction
  4. 4
    Sonstigereached 110° C

Vorschrift

A three-neck flask equipped with a reflux condenser, stirring rod and thermometer was charged with 14 grams of allylamine (0.25 mole), 41 grams of triethoxy silane (0.25 mole), 20 ml. of p-xylene and 0.1% by mole (calculated as rhodium), per mole of triethoxysilane, of [Rh(μ-P Ph2) (COD)]2, that is [rhodium(μ-diphenyl phosphide) (1,5-cyclooctadiene) dimer], and heated on an oil bath maintained at a temperature of 110° C. About 1 hour after the beginning of the reaction, the reaction temperature reached 110° C. At the end of the period the reaction mixture was subjected to gas chromatography analysis. It was found that gamma-aminopropyl triethoxy silane was obtained in a yield of 81% on an allylamine basis, while the yield of beta-aminopropyl triethoxy silane was 0.7% on a triethoxy silane basis.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04897501uspto-grants-1990_01