HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 2-Benzyloxy-6-bromopyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Product | 2-Benzyloxy-6-bromopyridine | HCID 817475 | 76% |
Reaction Steps
2,6-Dibromopyridine was condensed with benzyl alcohol by Ullmann reaction to obtain 2-benzyloxy-6-bromopyridine (yield 76%). This was further condensed with m-cresol by Ullmann reaction to obtain 2-benzyloxy-6-(3-methylphenoxy)-pyridine (yield 83%), which was then subjected to catalytic reduction in the presence of a catalyst, 5% palladium-carbon, to obtain 6-(3-methylphenoxy)-2-pyridone (yield 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05322845 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-51cb2f199786405ca003de1b23808b24 |
| Source note | uspto-grants-1994_06 |