HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174715Generated: November 2, 2026
2-Fluoropyridine → 2-((4-Bromobenzyl)oxy)pyridine
https://huagongshe.com/reaction/1174715
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluoropyridine | HCID 9746 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 4-Bromobenzyl alcohol | HCID 70119 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-((4-Bromobenzyl)oxy)pyridine | HCID 24799160 | — |
Reaction Steps
A mixture of 2-fluoropyridine (1.6 g), 4-bromobenzyl alcohol (3.08 g), potassium tert-butoxide (2.03 g) and N-methylpyrrolidone (12.8 ml) was heated at 100° C. by microwave irradiation for one minute. The mixture was diluted with water and extracted with ethyl acetate. The organic phase was dried over magnesium sulfate, filtered and concentrated. 2-(4-Bromobenzyloxy)pyridine was obtained in this way.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07838547B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-d45e013231954f7693c80ae667f949a7 |
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| Source note | uspto-grants-2010_11 |
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