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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388552Generated: October 30, 2026

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

https://huagongshe.com/reaction/1388552

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 suspension 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 under room temperature and 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 obtain 5.6 g of 4-chloro-2-fluoro-5-isopropoxyphenylaniline. nD24.5 1.5360.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04431822
Source datasetuspto-grants-1984_02
ORD IDord-87d7f3159eb9423fa3ce616eaed7a80d
Source noteuspto-grants-1984_02