HuagongsheHuagongshe Chemistry Print Report · For research reference only
Fluorobenzene → 4-Bromo-2-fluoro-1,1'-biphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Fluorobenzene | HCID 10008 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 4-Bromo-2-fluoro-1-iodobenzene | HCID 2724516 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Bromo-2-fluoro-1,1'-biphenyl | HCID 521063 | 10% |
Reaction Steps
Using methodology generally similar to the above examples, 1.22 g of phenylboronic acid in about 5 ml of ethanol, 3 g of 2-fluoro-4-bromoiodobenzene, 20 g of fluorobenzene, 0.2 g of 5% Pd on carbon catalyst, and 10 ml of 2 molar Na2CO3 were combined and stirred rapidly (without a nitrogen purge) at 25° C. for 65 hours. The desired 2-fluoro-4-bromobiphenyl was produced in about 10% yield with only partial conversion of the starting materials, considerable byproduct formation, but no observed terphenyl formation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05254776 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-7d0e5e7273064dd2a4ce390c8198263c |
| Source note | uspto-grants-1993_10 |