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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731472Generated: October 31, 2026

4-Chloro-2-fluoro-5-isopropoxy-nitrobenzene → 4-Chloro-2-fluoro-5-isopropoxyphenylaniline

https://huagongshe.com/reaction/1731472

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-fluoro-5-isopropoxy-nitrobenzeneHCID 13108986—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
Product4-Chloro-2-fluoro-5-isopropoxyphenylanilineHCID 5376338769.3%

Reaction Steps

A mixture of 4-chloro-2-fluoro-5-isopropoxynitrobenzene (13.5 g) and platinum dioxide (0.4 g) in ethanol (300 ml) was subjected to catalytic reduction with hydrogen at room temperature (ca. 20° C.) under atmospheric pressure, whereby a designed amount of hydrogen was absorbed. The resultant mixture was filtered to remove insoluble materials, and the filtrate was concentrated. The residue was subjected to purification by silica gel chromatography to give 5.6 g of 4-chloro-2-fluoro-5-isopropoxyphenylaniline. nD24.5 1.5360.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04622063
Source datasetuspto-grants-1986_11
ORD IDord-3fd52aa1c35a4379beaf1fd1d5042ccc
Source noteuspto-grants-1986_11