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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295939Generated: October 29, 2026

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

https://huagongshe.com/reaction/2295939

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 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 numberUS04427438
Source datasetuspto-grants-1984_01
ORD IDord-b8453d9918ef48f89528530a37a63316
Source noteuspto-grants-1984_01