HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915678Generated: October 25, 2026
p-Fluoronitrobenzene → Methyl 5-(4-nitrophenoxy)pyridine-3-carboxylate
https://huagongshe.com/reaction/1915678
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 5-hydroxypyridine-3-carboxylate | HCID 354317 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5-(4-nitrophenoxy)pyridine-3-carboxylate | HCID 22040734 | — |
Reaction Steps
The mixture containing methyl-5-hydroxypyridine-3-carboxylate (1 eq), Potassium bis(trimethylsilyl)amide (1.2 eq) was stirred in N,N-dimethylformamide for 2 hours at room temperature. To this mixture was added 1-fluoro-4-nitrobenzene (1.1 eq) and Potassium carbonate (1.2 eq) and stirred at 80° C. for 16 h. The reaction mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was separated and washed with brine, dried, filtered and concentrated in vacuum to give brown solid. Purification on silica gel methyl-5-(4-nitrophenoxy)pyridine-3-carboxylate. MS: MH+=274.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614330B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-024a47f96e074f53b5c094ac4d1176b9 |
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| Source note | uspto-grants-2013_12 |
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