Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 21269265 | HCID 21269265 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21269271 | HCID 21269271 | 48.4% |
Reaction Steps
To a stirred solution of 6.0 parts of methyl 1-[3,4-dihydrospiro-[2H-1-benzopyran-2,1'-cyclopentan]-4-yl]-1H-imidazole-5-carboxylate mononitrate in 135 parts of methanol were added 3.2 parts of bromine. The mixture was stirred for 1 hour at room temperature. The reaction mixture was poured into water and the whole was made alkaline. The product was extracted with 1,1'-oxybisethane. The extract was dried, filtered and evaporated. The residue was converted into the nitrate salt in a mixture of 16 parts of 2-propanone and 40 parts of 2,2'-oxybispropane. The salt was filtered off and dried in vacuo, yielding 4.4 parts (48.4%) of methyl 1-(6-bromo-3,4-dihydrospiro-[2H-1-benzopyran-2,1'-cyclopentan]-4-yl)-1H-imidazole-5-carboxylate mononitrate; mp. 162.3° C. (compound 1.63).
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-c240cc8bbc664cfaaec6d88da77172ad |
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| Source note | uspto-grants-1989_03 |
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