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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081605Generated: November 1, 2026

1-[(4-Nitrophenyl)(phenyl)methyl]-1H-imidazole → 4-((1H-Imidazol-1-yl)(phenyl)methyl)aniline

https://huagongshe.com/reaction/2081605

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[(4-Nitrophenyl)(phenyl)methyl]-1H-imidazoleHCID 14174067—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product4-((1H-Imidazol-1-yl)(phenyl)methyl)anilineHCID 1417406999.1%

Reaction Steps

A solution of 39 parts of intermediate 42, namely 1-[(4-nitrophenyl)phenylmethyl]-1H-imidazole, in 240 parts of ethanol was hydrogenated at 3.105Pa and at room temperature with 20 parts of Raney nickel. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated, yielding 34.6 parts (99.1%) of 4-[(1H-imidazol-1-yl)phenylmethyl]-benzenamine (interm. 43). In a similar manner there were also prepared:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05185346
Source datasetuspto-grants-1993_02
ORD IDord-ac00b31b79604b238565a8b96c59a582
Source noteuspto-grants-1993_02