HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 1-Ethyl-5-methyl-3-(trifluoromethyl)-1H-pyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1,1,1-Trifluoro-2,4-pentanedione | HCID 73943 | — |
| Reactant | Hydrazine, ethyl-, ethanedioate (1:1) | HCID 96181 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Ethyl-5-methyl-3-(trifluoromethyl)-1H-pyrazole | HCID 14770651 | — |
Reaction Steps
A solution of 25.0 g (grams) (167 mmol) (millimoles) of ethylhydrazine oxalate in 50 mL (milliliters) of ethanol was added to a solution of 25.0 g (162 mmol) of 1,1,1-trifluoro-2,4-pentanedione in 200 mL of ethanol at ambient temperature with stirring. The mixture was heated to reflux with stirring for 18 hours and was then allowed to cool. The volatile components were removed by evaporation under reduced pressure and the residue obtained was taken up in 150 mL, of dichloromethane. The resulting solution was washed twice with 100 mL portions of water, dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure to obtain 19.1 g (66 percent of theory) of the title compound as an amber oil
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05763359 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-9c4d449a241b4a029ed0e7b97708c0f9 |
| Source note | uspto-grants-1998_06 |