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HRID 1750791Erstellt: 27. Oktober 2026

Ethyl Acetate → 3,5-Dichloro-4-(2,2,2-trifluoroethoxy)aniline

https://huagongshe.com/reaction/1750791

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktSodium HydroxideHCID 14798—
EduktStannous ChlorideHCID 24479—
Edukt1,3-Dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzeneHCID 13852227—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelMethanolHCID 887—
Produkt3,5-Dichloro-4-(2,2,2-trifluoroethoxy)anilineHCID 1385214694%

Reaktionsschritte

To a solution of 1,3-dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzene (1.90 g, 6.55 mmol) in MeOH (20 mL) and 12 N HCl (20 mL) at rt, SnCl2 (3.72 g, 19.66 mmol) was slowly added to it and then the reaction mixture was stirred overnight at rt. To the reaction mixture was slowly added 3N NaOH to pH=10 and then extracted with EA. The combined organic layers were washed with brine, dried over anhydrous Na2SO4, and concentrated under reduced pressure. The residue was purified by column chromatography over silica gel eluted with PE:EA (6:1) to provide 3,5-dichloro-4-(2,2,2-trifluoroethoxy)aniline (1.60 g, yield 94%) as pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09156860B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-98801440c4a840a58f592124dd379132
Quellennotizuspto-grants-2015_10