Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | HCID 21269267 | HCID 21269267 | — |
| Product | HCID 21269263 | HCID 21269263 | 20% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04813998 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-49a2673143614942b19375a0f5231003 |
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| Source note | uspto-grants-1989_03 |
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