Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-3-hydroxy-6-iodopyridine | HCID 10777417 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18799610 | HCID 18799610 | 61.4% |
Reaction Steps
To a solution of 2-chloro-6-iodo-3-pyridinol (500 mg, 1.96 mmol), and K2CO3 (690 mg, 5.0 mmol) in methanol (5 mL) was added benzyl bromide (510 mg, 3.0 mmol). The reaction was refluxed for 60 minutes and was allowed to cool to 22° C. The mixture was then concentrated in vacuo. The remaining solids were slurried in ethyl acetate and filtered. The filtrate was dried over MgSO4 and concentrated in vacuo to yield 416 mg (61%) of 2-chloro-3-benzyloxy-6-iodo-pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06043248 |
|---|
| Source dataset | uspto-grants-2000_03 |
|---|
| ORD ID | ord-889dbba3d8ff4aafbe08352cf6544e67 |
|---|
| Source note | uspto-grants-2000_03 |
|---|