HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 2-Benzyloxy-5-bromopyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Benzyloxy-5-bromopyridine | HCID 11108191 | — |
Reaction Steps
A mixture of 2,5-dibromopyridine (1.0 eq.), benzyl alcohol (1.3 eq.), KOH (2.4 eq.) and DB-18—C-6 (0.0 Seq.) in toluene (0.3M) was refluxed for 3 h, then stirred overnight at rt. The mixture was concentrated, poured in water and extracted with Tol (2×). The combined organic extracts were dried over MgSO4, filtered and concentrated. Recrystallization in Hex:Et2O afforded the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07153968B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-6ff666849f224191a29269fd96a3ea6e |
| Source note | uspto-grants-2006_12 |