HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → 1-[1-(4-Fluorophenyl)-2-methylsulfonylethylidene]-2-methylhydrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 1-(4-Fluorophenyl)-2-(methylsulfonyl)-1-ethanone | HCID 1488246 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[1-(4-Fluorophenyl)-2-methylsulfonylethylidene]-2-methylhydrazine | HCID 86689353 | 31.9% |
Reaction Steps
To a 50 ml volume three-necked flask, 1-(4-fluorophenyl)-2-methylsulfonylethan-1-one (7-2-3) (5.0 g), methylhydrazine (14-a) (1.2 g), and ethanol (17.1 ml) were added under a nitrogen atmosphere, and heated to reflux for 4 hours. After the mixture was cooled, the precipitated solid was removed by filtration. The filtrate was concentrated under reduced pressure. To the residue was added hot hexane to be dissolved. The mixture was left to cool. Then, the precipitated crystals were collected by filtration, washed, and dried under reduced pressure. The crystal was purified by recrystallization (methanol) to give 1.8 g of 1-[1-(4-fluorophenyl)-2-methylsulfonylethylidene]-2-methylhydrazine (5-2-4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040709B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-cc869fd4b94f4b5687ea8069803c61f7 |
| Source note | uspto-grants-2015_05 |