HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-(2-Nitro-3-phenylbenzofuran-5-yl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Nitrogen oxide (N2O4) | HCID 25352 | — |
| Reactant | 4-(3-Phenylbenzofuran-5-yl)benzoic acid | HCID 23455894 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-(2-Nitro-3-phenylbenzofuran-5-yl)benzoic acid | HCID 12902867 | — |
Reaction Steps
A solution of 3.1 g. (0.01 mole) of the product of step D and 2 g. of dinitrogen tetraoxide in 250 ml. of chloroform is stirred at about 20° C. for about 16 hours. Evaporation of the mixture provides a residue which is dissolved in 10 percent sodium hydroxide solution, then acidified with hydrochloric acid. The precipitate is collected by filtration, dissolved in a chloroform/ethanol mixture and chromatographed on silica gel, eluting with chloroform. The solid obtained is recrystallized twice from a mixture of water and N,N-dimethylformamide to provide yellow crystals of 4-(2-nitro-3-phenylbenzofuran-5-yl)benzoic acid, m.p. 259°-261° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04258213 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-2f2e1cf6295e4bb59c5f958e86004c06 |
| Source note | uspto-grants-1981_03 |