HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromopyridine → 3-Bromo-2,6-dimethylphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | Decylamine | HCID 8916 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Bromo-2,6-dimethylphenol | HCID 12673511 | — |
Reaction Steps
For example, bromo pyridine (Apollo) 11.6 is treated with amine 10.7 in the presence of cesium carbonate in THF or alternative solvent at reflux to give the amine 11.7. The amine is then converted to the sulfonyl chloride 11.9 through the intermediate chloride 11.8 as described in Scheme 10. Using the above procedures, but employing, in place of the amino alkyl phosphonate 10.7, different alkyl phosphonates 10.6, and in place of the pyridine 11.6 different halo pyridines 11.1, the corresponding products 6.3 are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07649015B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-e3c22f2f97ff4bcaa09756e46c1b834b |
| Source note | uspto-grants-2010_01 |