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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248332Generated: October 30, 2026

Nitric Acid → 1-[(3-methoxy-4-nitrophenyl)methyl]-1H-imidazole

https://huagongshe.com/reaction/2248332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium HydroxideHCID 14923—
Reactant1-[(3-methoxyphenyl)methyl]-1H-imidazole mononitrateHCID 67868083—
Product1-[(3-methoxy-4-nitrophenyl)methyl]-1H-imidazoleHCID 1499070140.3%

Reaction Steps

To 184 parts of cold (10° C., ice bath) concentrated sulfuric acid were added portionwise 75 parts of 1-[(3-methoxyphenyl)methyl]-1H-imidazole mononitrate during 1 hour. Upon complete addition, stirring was continued for 30 minutes at 10° C. 15 Parts ofconcentrated nitric acid were added dropwise during 30 minutes at 15° C. Uponcompletion, the whole was stirred for 30 minutes at 10° C. The reaction mixture was poured into 1500 parts of crushed ice and the whole was treatedwith an ammonium hydroxide solution. The product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of ethyl acetate, methanol and methanol, saturated with ammonia, (95:2.5:2.5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated in vacuo. The residue was stirred in 45 parts of ethyl acetate. The precipitated product was filtered off, washed with 2,2'-oxybispropane and dried, yielding 28.2 parts (40.3%) of 1-[(3-methoxy-4-nitrophenyl)methyl]-1H-imidazole (int. 145).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05039677
Source datasetuspto-grants-1991_08
ORD IDord-408d9e378bc244a8b9d95fe960d323e8
Source noteuspto-grants-1991_08