HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylene Glycol → Azafluorene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylene Glycol | HCID 8117 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 9H-Indeno(2,1-b)pyridin-9-one | HCID 42613 | — |
| Reactant | Magnesium;2,3,4,5,6-pentahydroxyhexanal;sulfate | HCID 21924827 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Azafluorene | HCID 12226515 | 66.6% |
Reaction Steps
4.6 g (25.4 mmole) of 1-azafluoren-9-one was added to a solution of 9 ml (0.28 mole) of hydrazine and 50 ml of diethyleneglycol. Heating was started and the temperature was kept at 100° for 15 minutes, then raised to 195° and kept there for 1 hr. TLC showed the reaction was complete. The reaction solution was cooled to below 100° and poured into 300 ml of ice water. The aqueous phase was saturated with salt and extracted with 8×100 ml ether. The ether was dried with sodium sulfate and evaporated to yield 3.73 g of crude product. This was dissolved in hexane and treated with Magnesol, filtered and evaporated and finally recrystallized from hexane to yield 2.83 g of pure 1-azafluorene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05300642 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-2c90c633afb64ef791319d40d0c74bd2 |
| Source note | uspto-grants-1994_04 |