HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 4-Bromo-2,6-difluoropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2,6-Difluoropyridine-4-boronic acid | HCID 2762747 | — |
| Reactant | 2,6-Difluoro-4-hydrazinylpyridine | HCID 12175810 | — |
| Product | 4-Bromo-2,6-difluoropyridine | HCID 22015559 | — |
Reaction Steps
The second step in the synthetic procedure used in synthesizing the 2,6-difluoropyridin-4-ylboronic acid involves bromination of 2,6-difluoro-4-hydrazinopyridine by elemental bromine to produce 4-bromo-2,6-difluoropyridine. This reaction can be depicted as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07485725B1 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-178d2f65bba74d9ea9cd76ace67e8497 |
| Source note | uspto-grants-2009_02 |