HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382920Generated: October 31, 2026
Potassium Carbonate → HCID 18459338, compound
https://huagongshe.com/reaction/382920
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | Potassium 4-nitro-3-benzyloxyphenoxide | HCID 11781031 | — |
| Reactant | 2-(4-Benzyloxycarbonylphenoxy)-1-trifluoromethyl-3,4,5,6-tetrafluorobenzene | HCID 18459336 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 18459338 | HCID 18459338 | 94% |
Reaction Steps
40 g of the 2-(4-benzyloxycarbonylphenoxy)-1-trifluoromethyl-3,4,5,6-tetrafluorobenzene (0.09 mol) prepared as described in Example 9 and 25.5 g of potassium 4-nitro-3-benzyloxyphenoxide (0.09 mol) are dissolved in 400 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 and 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 allowed to cool to room temperature and is filtered through a fluted filter. The crude product is extracted 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: 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310238B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-db7e778c4dcf4d228e143bedc8a86bef |
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| Source note | uspto-grants-2001_10 |
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