HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952260Generated: November 2, 2026
Sodium Dithionite → 2-Methyl-5-n-propyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline
https://huagongshe.com/reaction/1952260
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Perfluoroisopropyl iodide | HCID 33978 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Methyl-5-propylaniline | HCID 19798278 | — |
| Catalyst | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | water MeOtBu | HCID 23212559 | — |
| Product | 2-Methyl-5-n-propyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline | HCID 86629854 | 90% |
Reaction Steps
5-n-Propyl-2-methylaniline (14.9 g, 0.1 mol) was diluted in a mixed solvent (300 ml) of tert-butyl methyl ether-water (1:1), and heptafluoroisopropyl iodide (29.6 g, 0.1 mol), tetrabutylammonium hydrogen sulfate (3.4 g, 0.01 mol), sodium hydrogen carbonate (8.4 g, 0.1 mol) and sodium dithionite (17 g, 0.1 mol) were successively added. The mixture was stirred overnight at room temperature. The reaction mixture was diluted in hexane, washed twice with 3N hydrochloric acid, and washed with aqueous sodium hydrogen carbonate and saturated brine. The organic layer was dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel chromatography (hexane:ethyl acetate 5:1) to give the desired compound (28.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404861B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-d85b36a4f17f48ce9b63166313a8d5cc |
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| Source note | uspto-grants-2013_03 |
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