HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexene → HCID 178526908, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | Nitrogen oxide (N2O4) | HCID 25352 | — |
| Reactant | HCID 178419493 | HCID 178419493 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178526908 | HCID 178526908 | — |
Reaction Steps
To a stirred solution of 1.9 g. (0.005 mole) of 2-bromo-3-phenyl-5-tetrazolylmethylbenzofuran in 50 ml. of warm acetic acid and 1 ml. of cyclohexene is added 1 g. of dinitrogen tetraoxide. The mixture is heated on a steam bath for 30 minutes, then cooled to ice bath temperature. The product is separated by filtration, washed with acetic acid and diethyl ether and recrystallized from ethanol to provide yellow needles of 2-nitro-3-phenyl-5(1H-tetrazol-5-ylmethyl)benzofuran, m.p. 245°-247° C. having the structure ##STR38##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04526896 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-a491d150faae4cb1b900f81a2e888914 |
| Source note | uspto-grants-1985_07 |