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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium DithioniteHCID 24489—
ReactantPerfluoroisopropyl iodideHCID 33978—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Methyl-5-propylanilineHCID 19798278—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventHexaneHCID 8058—
Solventwater MeOtBuHCID 23212559—
Product2-Methyl-5-n-propyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]anilineHCID 8662985490%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404861B2
Source datasetuspto-grants-2013_03
ORD IDord-d85b36a4f17f48ce9b63166313a8d5cc
Source noteuspto-grants-2013_03