Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | 2,5-Difluoroaniline | HCID 67775 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 18960027 | HCID 18960027 | 66.6% |
Reaction Steps
2,5-Difluoroaniline (38 g) was dissolved in acetic acid (120 ml), and then pyridine (25 g) was added thereto, followed by stirring. A mixed solution of iodine monochloride (50 g) with acetic acid (30 ml) was added dropwise thereto. After stirring at room temperature for 1 hour, the mixed solution was further stirred at 70° to 80° C. for 2 hours. Then, the reaction solution was poured into water, and the precipitated crystals were filtered, followed by washing with water. The resulting crystals were dissolved in chloroform, and then washed with water twice, further with 10% potassium hydroxide aqueous solution twice, and furthermore with water twice, followed by distilled off chloroform therefrom. The residue was distilled under reduced pressure (b.p. 130° to 140° C./20 mmHg), and then recrystallized from methanol, to give 4-iodo-2,5-difluoroaniline (50 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05356558 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-862af2edb0474ad0b950fa0f9ce78f1e |
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| Source note | uspto-grants-1994_10 |
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