HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bicarbonate Ion → 2-(2-Bromoethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bicarbonate Ion | HCID 769 | — |
| Reactant | 2-(2-Hydroxyethyl)pyridine | HCID 7675 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(2-Bromoethyl)pyridine | HCID 12913858 | 173.2% |
Reaction Steps
To an ice-cold solution of 2-pyridin-2-yl-ethanol (1 g, 8.1 mmol) in diethyl ether (20 mL) was added freshly distilled phosphorous tribromide (0.75 g, 2.7 mmol) over 15 min. The reaction mixture was warmed to r.t. and stirred for a further 5 hours. The reaction mixture was poured into an excess of cooled bicarbonate solution and extracted with dichloromethane (×2). The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated to afford 2-(2-bromo-ethyl)-pyridine (0.87 g, 58%) as a liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08604029B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-9a5e976d99864c469dd9014c1b2243cb |
| Source note | uspto-grants-2013_12 |