HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525998Generated: October 25, 2026
Iodopentafluoroethane → 5-(Perfluoroethyl)pyridin-2-amine
https://huagongshe.com/reaction/525998
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodopentafluoroethane | HCID 9636 | — |
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 5-(Perfluoroethyl)pyridin-2-amine | HCID 49853555 | 7% |
Reaction Steps
To a solution of 2-aminopyridine (25.0 g, 263 mmol) in a mixture of water (250 ml) and tert-butyl methyl ether (25 ml) was added, successively perfluoroethyl iodide (80 g, 38 ml, 315 mmol), sodium hydrosulfite (64.6 g, 26 ml, 315 mmol), sodium hydrogen carbonate (26.5 g, 315.6 mmol) and tetrabutyl ammonium hydrogen sulfate (“TBAHS”) (0.11 equiv., 9.92 g, 28.9 mmol). The reaction mixture was stirred at ambient temperature for 16 h. The mixture was filtered and the filtrate was extracted twice with tert-butyl methyl ether. The combined organic phases were washed successively with water, aqueous hydrochloric acid (1N) and brine, dried over sodium sulfate and concentrated. The residue was purified by flash chromatography (AcOEt/cyclohexane) to give 5-(1,1,2,2,2-pentafluoroethyl)pyridin-2-amine in 7% yield. 1H NMR (400 MHz, CDCl3) 8.23 (d, 1H), 7.61 (d, 1H), 6.72 (m, 1H), 5.04 (sb, 2H, NH2) ppm. The major by-product was 3,5-bis(1,1,2,2,2-pentafluoroethyl)pyridin-2-amine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09345244B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-de29af16b93140d58208adafbb6ed116 |
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| Source note | uspto-grants-2016_05 |
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