Reaktion #323814

ord-4916c91e18e84e1eb2f1fcf43cd6af01

Reaktionsgleichung

CCO[Si](CCCN)(OCC)OCC
3-aminopropyltriethoxysilane
COC(=O)NN
methyl hydrazinocarboxylate
CCO[Si](CCCNC(=O)NN)(OCC)OCC
4-(3-Triethoxysilylpropyl)Semicarbazide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.DISTILLATIONof distillate had been collected
  2. 2
    Temperaturthe reaction mass was cooled
  3. 3
    SonstigeThe pale yellow oil was decanted from the small amount of white solid

Vorschrift

A mixture of 44.2 g (0.20 mole) 3-aminopropyltriethoxysilane and 18.0 g (0.20 mole) methyl hydrazinocarboxylate under nitrogen was gradually heated to 150° C. with a slow distillation of the evolved methanol/ethanol from the reaction. After 2 hours at 150° C., 9.1 g. of distillate had been collected, and the reaction mass was cooled to ambient. The pale yellow oil was decanted from the small amount of white solid; yield 51 g (91%). IR (neat) 3320, 1640 (br), 1540 (br), 1070 (br), 940, 790 cm-1. NMR (CDCl3) 0.4-1.0 (m; 2H), 1.2 (t; 9H), 1.3-2.0 (m; 2H), 2.9-3.5 (m; 2H), 3.5-4.1 (m; 8H), 6.3 (br; 2H) ppm.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04645846uspto-grants-1987_02