HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304999Generated: October 27, 2026
Pentafluoropyridine → 2-(4-Benzyloxycarbonylphenoxy)-3,4,5,6-tetrafluoropyridine
https://huagongshe.com/reaction/2304999
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentafluoropyridine | HCID 69690 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | Potassium 4-benzyloxycarbonylphenoxide | HCID 23672351 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Benzyloxycarbonylphenoxy)-3,4,5,6-tetrafluoropyridine | HCID 18459337 | 91% |
Reaction Steps
33.8 g of pentafluoropyridine (0.2 mol) are dissolved in 500 ml of dimethylformamide, the solution is cooled to OC by means of a cryostat, and a solution of 53.3 g of potassium 4-benzyloxycarbonylphenoxide (0.2 mol) in 400 ml of dimethylformamide is then added dropwise over the course of 2 hours. After 24 hours at 0° C., the potassium salt has reacted. The dimethylformamide is then removed in a rotary evaporator, the residue is taken up in a little tetrahydrofuran, and the solution is filtered through a silica-gel column. The clear solution obtained is evaporated in a rotary evaporator until the reaction product precipitates out. The reaction product is then stirred in n-hexane, filtered off via a fluted filter and then dried for 48 hours under nitrogen at 40° C./10 mbar in a vacuum drying cabinet (yield: 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06437178B2 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-ac4e88d649814939b7b5b9123e4f502e |
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| Source note | uspto-grants-2002_08 |
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