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HRID 70808Erstellt: 23. Oktober 2026

Sodium Dithionite → 1-(1-Bromo-1,1,2,3,3,3-hexafluoropropan-2-yl)-6-(difluoromethoxy)aniline

https://huagongshe.com/de/reaction/70808

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium DithioniteHCID 24489—
Edukt1,2-Dibromo-1,1,2,3,3,3-hexafluoropropaneHCID 69579—
EduktSodium BicarbonateHCID 516892—
Edukt2-(Difluoromethoxy)anilineHCID 934620—
KatalysatorTetrabutylammonium hydrogen sulfateHCID 94433—
LösungsmittelWaterHCID 962—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
Produkt1-(1-Bromo-1,1,2,3,3,3-hexafluoropropan-2-yl)-6-(difluoromethoxy)anilineHCID 8667296526%

Reaktionsschritte

2-(Difluoromethoxy)aniline (1280 mg) and 1,2-dibromo-1,1,2,3,3,3-hexafluoropropane (8610 mg) were dissolved in tert-butylmethyl ether (30 ml) and water (30 ml), and added with tetrabutylammonium hydrogen sulfate salt (270 mg), sodium hydrogen carbonate (2030 mg) and sodium dithionite (4200 mg) in order. The mixture was stirred vigorously at room temperature for 2 days. The reaction solution was extracted twice with ethyl acetate. The organic phases were combined and washed with water, and dried over anhydrous magnesium sulfate. The drying agent was filtered off and the solvent was removed by distillation under the reduced pressure. The resulting residues were purified by column chromatography to obtain 1-(1-bromo-1,1,2,3,3,3-hexafluoropropan-2-yl)-6-(difluoromethoxy)aniline (810 mg, 26%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822691B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-f84e546fae6a492f91ed5477249a305d
Quellennotizuspto-grants-2014_09