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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976316Generated: October 30, 2026

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

https://huagongshe.com/reaction/976316

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 numberUS05612354
Source datasetuspto-grants-1997_03
ORD IDord-4c1e2e18d65c4daba7eb29b32769edca
Source noteuspto-grants-1997_03