HuagongsheHuagongshe Chemistry Print Report · For research reference only
Biphenyl → Silane, trichloro(9H-fluoren-9-ylmethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Biphenyl | HCID 7095 | — |
| Reactant | Silane, trichloro(1,2-dichloroethyl)- | HCID 79093 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Silane, trichloro(9H-fluoren-9-ylmethyl)- | HCID 12065632 | 38.9% |
Reaction Steps
In a 250 ml, three-necked, frame dried, round bottom flask, aluminum 0.40 g (15 mmol), biphenyl 20.0 g (130 mmol), and (1,2-dichloroethyl)- trichlorosilane 7.50 ml (53.5 mmol) were reacted as in Example 1 at 120° C. for 30 min. Freshly distilled hexane (60 ml) was added to the reaction mixture and insoluble solids in hexane were filtered from the organic solution. After hexane was distilled, the reaction products were vacuum distilled to give 6.53 g of 9-(trichlorosilyl)methylfluorene (bp; 130°-135° C./0.2 torr, yield; 18%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05847182 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-8c55fb26c72747aeb7123249a869ebe3 |
| Source note | uspto-grants-1998_12 |