HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183487Generated: November 2, 2026
Ethylene Oxide → 2-(6-Bromopyridin-3-yl)ethanol
https://huagongshe.com/reaction/2183487
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(6-Bromopyridin-3-yl)ethanol | HCID 22473220 | 40.2% |
Reaction Steps
BuLi (32.2 ml of a 1.6 M solution in hexanes, 52 mmol) added dropwise to a stirred solution of 2,5-dibromopyridine (11.09 g, 46.8 mmol) in Et2O (400 ml) at −78° C. under nitrogen. Upon complete addition the reaction mixture was stirred for 45 min and then a solution of ethylene oxide (6.74 g, 0.14 mol) in THF (70 ml) was added. The reaction mixture was warmed to room temperature, stirred for 1 h and then quenched by addition of NH4Cl solution (sat., 150 ml). The organics were extracted with EtOAc (3×100 ml), washed with brine (100 ml) and dried (MgSO4). The material was concentrated under reduced pressure, whilst simultaneously dry-loading onto silica. The material was purified by column chromatography on silica eluting with Et2O and then EtOAc to give the pure alcohol (3.8 g, 40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06900209B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-f3eef6c20b214f90a1dee85df08a484c |
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| Source note | uspto-grants-2005_05 |
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