HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenothiazine → (3-Aminopropyl)triethoxysilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenothiazine | HCID 7108 | — |
| Reactant | Allylamine | HCID 7853 | — |
| Reactant | Triethoxysilane | HCID 13830 | — |
| Product | (3-Aminopropyl)triethoxysilane | HCID 13521 | 65% |
Reaction Steps
571 parts of allylamine, 0.38 part of [Rh(NBD)2 ](+). BF4(-) (note: NBD: Norbornadiene), 1.0 part of phenothiazine and 1640 parts of triethoxysilane were charged into a sealed tube and allowed to react in an oil bath for 2 hours at 130° C. Following cooling, the product was analyzed with gas chromatography. Aminopropyltriethoxysilane was produced at a yield of 65% and moreover, the ratio of γ:β isomer was 24:1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04927949 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-d90c2125541648e1aa53f5c13e51d10e |
| Source note | uspto-grants-1990_05 |