HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 1-butyl-5-methyl-1H-pyrazole-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | ethyl 1-butyl-5-methyl-1H-pyrazole-3-carboxylate | HCID 66958271 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-butyl-5-methyl-1H-pyrazole-3-carboxamide | HCID 66958958 | — |
Reaction Steps
A solution of ethyl 1-butyl-5-methyl-1H-pyrazole-3-carboxylate (18.1 g, 86.1 mmol) in methanol (25 mL) was treated with ammonium hydroxide (25 mL) according to a modification of the method described in Part D of Examples 1-4. At the end of the reaction, the methanol was removed under reduced pressure, and the remaining solution was cooled in a refrigerator. A precipitate formed, was isolated by filtration, and was washed with water. The solid (9 g) was recrystallized from hexane (300 mL) and ethyl acetate (30 mL), isolated by filtration, washed with hexane, and air-dried to provide 6.95 g of 1-butyl-5-methyl-1H-pyrazole-3-carboxamide as colorless plates, mp 113.5-114.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879849B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-5065ce42aaab450d84aa5c6470bb1b81 |
| Source note | uspto-grants-2011_02 |