HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,3,3-Trifluoropropyl-trimethoxysilane → 3,3,3-Trifluoropropyl(cyclopentyl)dimethoxysilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,3,3-Trifluoropropyl-trimethoxysilane | HCID 67933 | — |
| Reactant | Silane hexane | HCID 131717238 | — |
| Reactant | HCID 178478989 | HCID 178478989 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3,3,3-Trifluoropropyl(cyclopentyl)dimethoxysilane | HCID 19900045 | — |
Reaction Steps
Under nitrogen, a 500 ml Schlenk flask was cooled to room temperature, charged with 150 ml of diethyl ether and cyclopentylmagnesium chloride (0.055 mol, 27.7 ml) and warmed slightly to 30° C. A 100 ml Schlenk flask was purged with nitrogen and charged with 75 ml hexane and 3,3,3-trifluoropropyltrimethoxy silane (10 ml, 0.0504 mol). The silane/hexane solution was added dropwise via cannula to the Grignard/diethyl ether mixture producing a white cloudy mixture. After addition (1.25 hrs.), the Grignard containing flask was rinsed once with 25 ml of hexane. The reaction mixture was stirred at room temperature for one hour.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05102842 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-dc2a1dd5867444178c2fa5cf1148e5a1 |
| Source note | uspto-grants-1992_04 |