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 | US05434264 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-f937471d2f134a0aaa388176d5a3b2cb |
| Source note | uspto-grants-1995_07 |