HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Dinitrophenol → 4-(3,4-Dinitro-phenoxy)-quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Dinitrophenol | HCID 11348 | — |
| Reactant | 4-Chloroquinoline | HCID 69140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-(3,4-Dinitro-phenoxy)-quinoline | HCID 17756076 | — |
Reaction Steps
4-Chloroquinoline (4.3 g, 26.3 mmol) and 3,4-dinitrophenol (41.5 g, 24.4 mmol) were heated at 150° C. for 30 min. The mixture was cooled to RT and the residue was dissolved in CH2Cl2. The mixture was diluted in NaOH 2 M and extracted with CH2Cl2. The organic phase was dried, filtered and evaporated. The residue was diluted in EtOAc and filtered through a silica pad. The solvent was removed to give the title compound as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531553B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-2e6b9db57ddb4976b59563a59f01828d |
| Source note | uspto-grants-2009_05 |