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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787083Generated: October 30, 2026

3-chloro-4-{4-[3-(1H-imidazol-1-yl)propyl]phenoxy}nitrobenzene → 3-chloro-4-{4-[3-(1H-imidazol-1-yl)propyl]phenoxy}aniline

https://huagongshe.com/reaction/1787083

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-chloro-4-{4-[3-(1H-imidazol-1-yl)propyl]phenoxy}nitrobenzeneHCID 67521304—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
Product3-chloro-4-{4-[3-(1H-imidazol-1-yl)propyl]phenoxy}anilineHCID 6752115445.2%

Reaction Steps

To a solution of 3-chloro-4-{4-[3-(1H-imidazol-1-yl)propyl]phenoxy}nitrobenzene (669 mg) in methanol (7 mL) was added 5% Pt/C (140 mg), and the mixture was stirred under hydrogen atmosphere at room temperature for 16 hrs. 5% Pt/C was filtered off and the filtrate was concentrated. The residue was purified by basic silica gel column chromatography (eluent, ethyl acetate:hexane=80:20→100:0) and further washed with diethyl ether and hexane to give the title compound (277 mg) as a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507740B2
Source datasetuspto-grants-2009_03
ORD IDord-9f3ea9e203b14268bbef232e96c7413e
Source noteuspto-grants-2009_03