HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358888Generated: November 1, 2026
Potassium Iodide → HCID 20067142, compound
https://huagongshe.com/reaction/358888
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoroethyl bromide | HCID 12982 | — |
| Reactant | HCID 20067155 | HCID 20067155 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20067142 | HCID 20067142 | 19.1% |
Reaction Steps
2.44 g (0.018 mole) of potassium carbonate, a catalytic amount of potassium iodide and 1.80 g (0.014 mole) of 2-fluoroethyl bromide were added to a solution of 3.00 g (0.012 mole) of 3,4-difluoro-2-methoxy-N-(trifluoroacetyl)aniline (XI) [prepared as described in Step (C1) above] dissolved in 50 ml of dimethylformamide. The mixture was then stirred at 65° C. for 5 hours. At the end of this time, the solvent was distilled off from the mixture under reduced pressure. The residue was extracted with ethyl acetate and purified by column chromatography through silica gel eluted with toluene, to give 0.69 g of 3,4-difluoro-N-(2-fluoroethyl)-2-methoxy-N-(trifluoroacetyl)aniline (XII, R9' =2-fluoroethyl) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04997943 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-2ee0fb421a764e4d9b41c780ca0819b7 |
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| Source note | uspto-grants-1991_03 |
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