HuagongsheHuagongshe Chemistry Print Report · For research reference only
Borane, dichlorophenyl- → Bis(indenyl) (phenyl)borane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Borane, dichlorophenyl- | HCID 136678 | — |
| Reactant | HCID 178506815 | HCID 178506815 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Bis(indenyl) (phenyl)borane | HCID 15873885 | 74.3% |
Reaction Steps
In 50 ml of diethyl ether, 5.01 g (31.5 mmol) of dichloro(phenyl)borane is cooled to -78° C. and a solution of 7.70 g (63.1 mmol) of indenyllithium in 50 ml of diethyl ether is added dropwise within one hour. After warming to room temperature, the mixture is filtered, and the slightly yellow filtrate is highly concentrated in vacuo. Gradual cooling from 0° C. to -20° C. results in the formation of 7.45 g (74%) of bis(indenyl) (phenyl)borane in the form of colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05962718 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-1714a656bb664564913f62337e3e4b1c |
| Source note | uspto-grants-1999_10 |