HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen oxide (N2O4) → 6,7-dihydro-2-nitro-3-phenyl-5H-indeno-[5,6-b]furan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen oxide (N2O4) | HCID 25352 | — |
| Reactant | 6,7-dihydro-3-phenyl-5 H-indeno-[5,6-b]furan | HCID 12866340 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6,7-dihydro-2-nitro-3-phenyl-5H-indeno-[5,6-b]furan | HCID 12866339 | — |
Reaction Steps
To a solution of 2.3 g. (0.01 mole) of the product of step B in 100 ml. of chloroform is added 1.8 g. (0.02 mole) of dinitrogen tetraoxide, and the mixture is stirred at about 20° C. for 20 hours. The mixture is evaporated, and the residue is triturated with isopropyl ether to provide a precipitate. The precipitate is separated by filtration and recrystallized from methanol to provide 6,7-dihydro-2-nitro-3-phenyl-5 H-indeno-[5,6-b]-furan, m.p. 161°-164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04260547 |
| Source dataset | uspto-grants-1981_04 |
| ORD ID | ord-89b5ec3b4570457f85b41063207960c1 |
| Source note | uspto-grants-1981_04 |