HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenyldimethoxysilane → Bisfluorenyldiphenylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenyldimethoxysilane | HCID 81284 | — |
| Reactant | 2,7-Dibromo-9,9-di-n-octylfluorene | HCID 5215321 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Bisfluorenyldiphenylsilane | HCID 21889331 | — |
Reaction Steps
Under a nitrogen gas atmosphere, 4.90 g (8.94 mmol) of 2,7-dibromo-9,9-dioctylfluorene, 20 ml of diethyl ether and 10 ml of toluene were added to a 100 ml three-necked flask equipped with a reflux condenser and a dropping funnel. Under cooling by an ice bath, 6.1 ml (9.76 mmol) of a hexane solution of n-butyllithium (1.6 M) was added dropwise. As the hexane solution of butyllithium was added dropwise, the solution turned red. The solution was agitated “as is” for approximately 1 hour; then, 1.03 g (4.21 mmol) of dimethoxydiphenylsilane was added, and this mixture was reacted under agitation all night.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135242B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-e611839db2254d5c9b9ab4899234630d |
| Source note | uspto-grants-2006_11 |