HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromobiphenyl → ([1,1'-Biphenyl]-4-yl)(tributyl)stannane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromobiphenyl | HCID 7101 | — |
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | ([1,1'-Biphenyl]-4-yl)(tributyl)stannane | HCID 57334235 | — |
Reaction Steps
2.5 M of n-BuLi (2.1 mL/hexane, 5.32 mmol) was added to 4-bromobiphenyl (1.24 g, 5.32 mmol/THF (20 mL)) and reacted at −78° C. for 40 minutes under a dry and anaerobic operation condition to form a solution. SnBu3Cl (1.65 mL, 5.85 mmol) was then added to the solution and reacted at −78° C. for 1 hour. After returning to room temperature, the solution was continuously reacted for 8 hours. After the reaction was completed, the solution was extracted by ether (30 mL) and deionized water (50 mL). An organic phase was collected. After removal of ether by a rotary concentrator, the organic phase was purified by reduced-pressure distillation to form a transparent colorless oily product (21, 1.83 g, 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759543B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-000adc2683c1418aa85492f8cfdf5de8 |
| Source note | uspto-grants-2014_06 |