HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethoxy(3-isocyanatopropyl)silane → HCID 53869758, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethoxy(3-isocyanatopropyl)silane | HCID 90613 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | 8-Cyclohexadecen-1-one | HCID 534634 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 53721826 | HCID 53721826 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 53869758 | HCID 53869758 | — |
Reaction Steps
1 ml of 3-isocyanatopropyltriethoxysilane and 50 mg of triethylamine are added to 0.9 g of 8-cyclohexadecen-1-ol, prepared by reduction of 8-cyclohexadecen-1-one using NaBH4 in ethanol, and the mixture is kept at 80° C. for 24 hours. Low-boiling components are removed at 90° C./0.1 mbar. The residue solidifies on cooling to form a wax and shows only traces of an isocyanate band in the IR spectrum, but instead a strong band (1700 cm-1) of the ##STR5## 5.2(m, 2H, --CH=CH--); 0.6 (m, --CH2Si).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05702777 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-083132ec92c44138bd75802dcf0f1929 |
| Source note | uspto-grants-1997_12 |