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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756520Generated: October 28, 2026

Imidazole → 1-[(4-Nitrophenyl)(phenyl)methyl]-1H-imidazole

https://huagongshe.com/reaction/1756520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant1-[Chloro(phenyl)methyl]-4-nitrobenzeneHCID 13541734—
SolventAcetonitrileHCID 6342—
Product1-[(4-Nitrophenyl)(phenyl)methyl]-1H-imidazoleHCID 1417406753%

Reaction Steps

To a stirred solution of 88.7 parts of 1-[chlorophenylmethyl]-4-nitrobenzene in 790 parts of acetonitrile were added 121.8 parts of 1H-imidazole. After stirring for 24 hours at reflux temperature, the reaction mixture was evaporated. The residue was taken up in methylbenzene. This solution was washed with K2CO3 (aq.), dried, filtered and evaporated. The residue was purified by column chromatography (silica gel; CH2Cl2 /CH3OH 98:2). The eluent of the desired fraction was evaporated, yielding 53 parts (53%) of 1-[(4-nitrophenyl)phenylmethyl]-1H-imidazole (interm. 42).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05441954
Source datasetuspto-grants-1995_08
ORD IDord-5e1bbb8d08d7427e82d2dd37fd50a945
Source noteuspto-grants-1995_08