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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750791Generated: October 25, 2026

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

https://huagongshe.com/reaction/1750791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantStannous ChlorideHCID 24479—
Reactant1,3-Dichloro-5-nitro-2-(2,2,2-trifluoroethoxy)benzeneHCID 13852227—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Product3,5-Dichloro-4-(2,2,2-trifluoroethoxy)anilineHCID 1385214694%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156860B2
Source datasetuspto-grants-2015_10
ORD IDord-98801440c4a840a58f592124dd379132
Source noteuspto-grants-2015_10