HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → 1-Methyl-4-(4-methylphenyl)-1H-pyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 2-(4-Methylphenyl)malondialdehyde | HCID 2736930 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Methyl-4-(4-methylphenyl)-1H-pyrazole | HCID 4319070 | 89.8% |
Reaction Steps
A mixture of 2-(4-methylphenyl)-malondialdehyde (3.05 g), absolute ethanol (40 ml), and methylhydrazine (1.09 g) was stirred at room temperature for 18 hours and the volatiles removed at room temperature. Water was added and the mixture was extracted with dichloromethane. After drying over anhydrous sodium sulfate, the solution was filtered through a short column of hydrous sodium magnesium silicate and further eluted with several volumes of dichloromethane. The combined organic phase was concentrated on a steam bath with the gradual addition of hexane until crystallization occurred. After cooling, the crystals were collected by filtration to yield the title compound (2.91 g), m.p. 107-108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06511974B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-f6371761bdcb4afd94be1f844baf2036 |
| Source note | uspto-grants-2003_01 |