HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 2-Bromo-6-phenoxypyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | 6-Phenoxy-2-pyridinemethanol | HCID 12879155 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-Bromo-6-phenoxypyridine | HCID 824589 | — |
Reaction Steps
The 6-phenoxy-2-pyridinylmethanol may be prepared by first reacting phenol with 2,6-dibromopyridine in dimethyl sulfoxide under basic conditions to give 2-bromo-6-phenoxypyridine. This compound is then reacted at -70° C. with n-butyllithium in diethyl ether and then with dimethylformamide at -30° C. to give 2-formyl-6-phenoxypyridine. This aldehyde is in turn reacted with sodium borohydride in methanol, yielding the corresponding 6-phenoxy-2-pyridinylmethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05223536 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-77d0eaf1f0104d8facd51eceb184f327 |
| Source note | uspto-grants-1993_06 |