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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202276Generated: October 30, 2026

Hydrochloric Acid → 4-(1-Ethoxy-2-methylpropan-2-yl)-3,5-difluoroaniline

https://huagongshe.com/reaction/2202276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-(1-ethoxy-2-methylpropan-2-yl)-3,5-difluoro-N,N-bis(4-methoxybenzyl)anilineHCID 118622715—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Product4-(1-Ethoxy-2-methylpropan-2-yl)-3,5-difluoroanilineHCID 11862276893.2%

Reaction Steps

A mixture of 4-(1-ethoxy-2-methylpropan-2-yl)-3,5-difluoro-N,N-bis(4-methoxybenzyl)aniline (8.51 g, 18.12 mmol), 1N hydrochloric acid (36.2 mL) and 10% palladium-carbon (1.929 g, 0.91 mmol, 50%, wet) in MeOH (164 mL) under hydrogen atmosphere (4 atm), and the mixture was stirred at room temperature for 1.5 hr. The catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure. The obtained residue was dissolved in ethyl acetate, and the solution was washed with 1N aqueous sodium hydroxide solution and brine, and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 5→20% ethyl acetate/hexane) to give 4-(1-ethoxy-2-methylpropan-2-yl)-3,5-difluoroaniline (3.87 g, 16.88 mmol, 93%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365520B2
Source datasetuspto-grants-2016_06
ORD IDord-976ff95b173a4142a13170aefcab8f65
Source noteuspto-grants-2016_06