HuagongsheHuagongshe Chemistry Print Report · For research reference only
((Chloromethyl)phenylethyl)-trimethoxysilane → HCID 178503001, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | ((Chloromethyl)phenylethyl)-trimethoxysilane | HCID 53426825 | — |
| Reactant | HCID 178473702 | HCID 178473702 | — |
| Reactant | HCID 178527894 | HCID 178527894 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178503001 | HCID 178503001 | 53% |
Reaction Steps
10 mmole of 3-mercapto-1H-1,2,4-triazole was dissolved in 20 ml ethanol, then 10 mmole EtOK was added, and stirred for 5 minutes. 10 mmole of ((chloromethyl)phenylethyl)trimethoxysilane was added to the solution, and stirred for 6 hours. The white precipitate was removed by filtration, the solvent in the filtrate was removed in vacuum. The obtained solid was dissolved in methanol, and separated with a Si gel column (solvents: 7 ethylacetate/3 hexane in volume). Yield: 53%. 1H NMR (CDCl3) of Precursors 6: δ(ppm) 8.09 (1H, s), 7.19 (4H, m), 4.29 (2H, s), 3.55 (9H, s), 2.72 (2H, t, JH-H=8.50), 1.02 (2H, t, JH-H=8.50).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07576165B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-14288d0c3f00407286a109f65d1ae6f4 |
| Source note | uspto-grants-2009_08 |