HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695528Generated: November 1, 2026
2-Fluoropyridine → 2-((4-Bromobenzyl)oxy)pyridine
https://huagongshe.com/reaction/1695528
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 | US08163741B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-d90561b0a0bc4163a1862f68761cfb56 |
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| Source note | uspto-grants-2012_04 |
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