HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → ethyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Reactant | (Dimethylaminomethylene)-3-oxobutanoate | HCID 86629460 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | ethyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate | HCID 13654177 | 65% |
Reaction Steps
In ethanol (10 mL) was placed the tert-butylhydrazine hydrochloride (1.35 g, 10.8 mmol) and ethyl 2-((dimethylaminomethylene)-3-oxobutanoate (2.00 g, 10.8 mmol). The mixture warmed to reflux and stirred for 2 hrs, cooled to RT and stirred overnight. The mixture was evaporated at reduced pressure to give an oil which was dissolved in ether (25 mL) and washed successively with water (25 mL), saturated sodium bicarbonate (25 mL) and brine (25 mL), dried (Na2SO4 and evaporated at reduced pressure to give an oil. The oil was purified by chromatography (Biotage S1-25 column, 10-40% ethyl acetate/Hex 750 mL) to give ethyl 1-tert-butyl-5-methyl-1H-pyrazole-4-carboxylate (1.48 g, 65% yield) as an oil. MS (ESI) m/z: 211.0 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897762B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-5676cb8321db4570b4f15d2f6209e294 |
| Source note | uspto-grants-2011_03 |