HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 2-Benzyloxy-6-bromopyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Catalyst | 18-Crown-6 | HCID 28557 | — |
| Product | 2-Benzyloxy-6-bromopyridine | HCID 817475 | — |
Reaction Steps
A stirred mixture of 2,6-dibromopyridine (3.55 g), benzyl. alcohol (1.63 g), potassium hydroxide (1.68 g), 18-Crown-6 (0.20 g) and toluene (25 ml) is heated under reflux for 30 minutes. The cool solution washed with water and brine, dried (MgSO4) and evaporated to give an oil which is vacuum-distilled (Kugelrohr) to give 3.85 g of 2-benzyloxy-6-bromopyridine, bp 220-225° C./1.0 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211220B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-93682894d27b42bb9ad767ec95113533 |
| Source note | uspto-grants-2001_04 |