HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 1-tert-butyl-5-methyl-1H-pyrazole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Reactant | HCID 86623854 | HCID 86623854 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 1-tert-butyl-5-methyl-1H-pyrazole-3-carboxylate | HCID 2800557 | 45% |
Reaction Steps
In ethanol (5 mL) was placed the t-butylhydrazine hydrochloride (0.79 g, 6.3 mmol) and ethyl 2-acetyl-3-(dimethylaminomethylene)acrylate (1.0 g, 6.3 mmol). The mixture was refluxed for 8 hours. The mix was evaporated at reduced pressure to give an oil. The oil was dissolved in ether (25 mL) and washed successively with water (25 mL), saturated sodium bicarbonate (25 mL) and brine (25 mL) was dried (Na2SO4), concentrated in vacuo and purified by silica gel column chromatography (EtOAc/hexanes) to obtain ethyl 1-tert-butyl-5-methyl-1H-pyrazole-3-carboxylate (0.60 g, 45% yield). 1H NMR (400 MHz, DMSO-d6): δ 6.54 (s, 1H), 4.22 (q, J=7.2 Hz, 2H), 2.44 (s, 3H), 2.42 (s, 3H), 1.57 (s, 9H), 1.25 (t, J=7.2 Hz, 3H); MS (ESI) m/z: 211.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143293B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-2557e3d52995472496a22fc614158656 |
| Source note | uspto-grants-2012_03 |