HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylaniline → 5,12-dihydro-benzo[b]phenazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2,3-Dihydroxynaphthalene | HCID 7091 | — |
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 5,12-dihydro-benzo[b]phenazine | HCID 352347 | 76% |
Reaction Steps
2,3-dihydroxynapthalene (10 g, 62.5 mmol), 1,2-phenylenediamine (6.75 g, 62.5 mmol) and N,N-dimethylaniline (54 ml) are placed into a round bottom flask under nitrogen atmosphere. Mixture is stirred at reflux. Reaction is monitored by TLC (CH2Cl2:Heptane/1:1) until all 2,3-dihydroxynaphthalene has reacted (˜3 hours). After cooling to room temperature, toluene (100 ml) is added and solid is collected by vacuum filtration. After washing with toluene (50 ml), ethanol (100 ml) and hexanes (50 ml), the product is dried under vacuum to yield 11.0 g (76% yield) of light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06919140B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-72553dac175d4c249ec39ffb81082647 |
| Source note | uspto-grants-2005_07 |