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 | Dibenzo-18-crown-6 | HCID 26541 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Benzyloxy-5-bromopyridine | HCID 11108191 | — |
Reaction Steps
A mixture of 2,5-dibromopyridine, benzyl alcohol (1.3 eq), potassium hydroxide pellets (2.4 eq) and dibenzo-18-crown-6 (0.05 eq) in toluene (4 ml/mmol) was refluxed with azeotropic removal of water for 3 hours. After evaporation of the toluene, the resulting mixture was partitioned between chloroform and water. The crude product from the organic phase was recrystallized from ether-hexane to afford the 2-Benzyloxy-5-bromopyridine compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07312334B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-0f6878ec9e8946c8805a90a2e6399a14 |
| Source note | uspto-grants-2007_12 |