HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxyethanol → 5-Bromo-2-(2-methoxyethoxy)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxyethanol | HCID 8019 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 5-Bromo-2-(2-methoxyethoxy)pyridine | HCID 22502717 | — |
Reaction Steps
0.25 mL 2-methoxyethanol (3.17 mmol) are added to a mixture of 80 mg (3.17 mmol) sodium hydride and 5 mL THF. The mixture is stirred at rt for 10 min. Subsequently, 500 mg (2.11 mmol) 2,5-dibromopyridine are added and the mixture is stirred for 5 h at 75° C. After that time, the reaction mixture is diluted with sat. aq. NaHCO3 solution and extracted with EtOAc. The organic layer is dried over magnesium sulphate and the solvent is removed in vacuo. The crude product is purified by column chromatography (silica gel, PE/EtOAc 85/15).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877754B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-fef4f21f5ac54b9189cbdb31ce4a5c00 |
| Source note | uspto-grants-2014_11 |