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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394491Generated: October 29, 2026

Aniline → 3,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)aniline

https://huagongshe.com/reaction/2394491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantHexafluoropropyleneHCID 8302—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Amino-2,6-dichlorophenolHCID 80037—
SolventTetrahydrofuranHCID 8028—
Product3,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)anilineHCID 9883878—
Product3,5-Dichloro-4-[(1,2,3,3,3-pentafluoro-1-propen-1-yl)oxy]benzenamineHCID 54491816—

Reaction Steps

To 1.1 liters of tetrahydrofuran containing 44.5 g of 2,6-dichloro-4-aminophenol and 3.2 g potassium hydroxide, was added subsurface 38.7 g of hexafluoropropene. The addition was complete in 25 minutes at a temperature of 8°-11° C. Analysis by liquid chromatography indicates no starting aniline present. Most of the THF was removed under vacuum, 500 mL water was added and the resulting mixture was extracted 3×500 mL ethyl ether. The combined extracts were washed with 2×100 mL 1N NaOH, 2×200 mL brine, dried over anhydrous sodium sulfate, filtered and the solvent removed under vacuum to give a mixture. This mixture was separated by prep LC to give 46.8 g of 3,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)aniline and ~4 g of 3,5-dichloro-4-(1 ,2,3,3,3-pentafluoropropenoxy) aniline . Proton and 19F nmr and mass spectra were consistent with the proposed structures.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811461
Source datasetuspto-grants-1998_09
ORD IDord-c75ea8e381164e50b68d49dfa1d420fa
Source noteuspto-grants-1998_09