HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305000Generated: October 27, 2026
Potassium Carbonate → HCID 18459339, compound
https://huagongshe.com/reaction/2305000
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 11781031 | HCID 11781031 | — |
| Reactant | 2-(4-Benzyloxycarbonylphenoxy)-3,4,5,6-tetrafluoropyridine | HCID 18459337 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 18459339 | HCID 18459339 | 92% |
Reaction Steps
40 g of the 2-(4-benzyloxycarbonylphenoxy)-3,4,5,6-tetrafluoropyridine prepared as described in Example 6 (0.106 mol) and 30 g of potassium 4-nitro-3-benzyloxyphenoxide (0.106 mol) are dissolved in 500 ml of dimethyl sulfoxide. 30 g of potassium carbonate (0.22 mol) are added in portions to the solution. The mixture is then stirred at room temperature for 24 hours, then heated at 60° C. for 24 hours, and 15 g of potassium hydrogencarbonate (0.15 mol) are then added. The reaction solution is then cooled to room temperature and filtered through a fluted filter. The crude product is washed by shaking with 300 ml of ethyl acetate and 700 ml of water, and the organic phase is washed three times with water and evaporated in a rotary evaporator until the reaction product precipitates out. The reaction product is then recrystallized from a mixture of ethyl acetate and n-hexane (volume ratio 1:1) and then dried for 48 hours under nitrogen at 40° C./10 mbar in a vacuum drying cabinet (yield: 92%).
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-39f3119ce2da43b18e60b986cbbd472d |
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| Source note | uspto-grants-2002_08 |
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