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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1194268Generated: November 2, 2026

Nitric Acid → HCID 21269263, compound

https://huagongshe.com/reaction/1194268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantHCID 21269267HCID 21269267—
ProductHCID 21269263HCID 2126926320%

Reaction Steps

A solution of 31 parts of methyl 1-(8-chloro-2,3-dihydro-4H-1-benzopyran-4-yl)-1H-imidazole-5-carboxylate mononitrate in 260 parts of a nitric acid solution 60% was stirred for 45 minutes at room temperature (exothermic reaction). The reaction mixture was poured into crushed ice and the whole was made alkaline. The product was extracted with trichloromethane. The undissolved product was filtered off (the trichloromethane layer was set aside) and dried, yielding a first fraction of 7 parts (20.0%) of methyl 1-(8-chloro-2,3-dihydro-6-nitro-4H-1-benzopyran-4-yl)-1H-imidazole-5-carboxylate mononitrate. The trichloromethane layer, which was set aside (see above), was washed with water, dried, filtered and evaporated. The residue was converted into the nitric acid salt. The product was filtered off and dried, yielding a second fraction of 21 parts (60.2%) of methyl 1-(8-chloro-2,3-dihydro-6-nitro-4H-1-benzopyran-4-yl)-1H-imidazole-5-carboxylate mononitrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04813998
Source datasetuspto-grants-1989_03
ORD IDord-49a2673143614942b19375a0f5231003
Source noteuspto-grants-1989_03