HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3-Aminopropyl)triethoxysilane → 4-(3-Triethoxysilylpropyl)Semicarbazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3-Aminopropyl)triethoxysilane | HCID 13521 | — |
| Reactant | Methyl carbazate | HCID 80519 | — |
| Solvent | Ethanol, mixt. with methanol | HCID 18681192 | — |
| Product | 4-(3-Triethoxysilylpropyl)Semicarbazide | HCID 20216498 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04645846 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-4916c91e18e84e1eb2f1fcf43cd6af01 |
| Source note | uspto-grants-1987_02 |