HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 2-Bromo-6-(1-bromo-2-fluoroethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-(6-Bromopyridin-2-yl)-2-fluoroethanol | HCID 59525900 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-6-(1-bromo-2-fluoroethyl)pyridine | HCID 59526254 | — |
Reaction Steps
1-(6-Bromopyridin-2-yl)-2-fluoroethanol (0.525 g, 2.39 mmol) and triphenylphosphine (1.252 g, 4.77 mmol) were taken up in DCM (25 mL). A solution of carbon tetrabromide (1.582 g, 4.77 mmol) in DCM (10 mL) was added and the resulting mixture stirred at room temperature overnight. The precipitate was removed by filtration and the filtrate concentrated in vacuo. Purification of the residue by silica gel column chromatography (0-10% EtOAc-hexanes) gave the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367706B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-3690968ecc6f47458254116afc17fff1 |
| Source note | uspto-grants-2013_02 |