HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930343Generated: November 2, 2026
Borane;tetrahydrofuran → ethyl 3-tert-butyl-1-(2-(dimethylamino)ethyl)-1H-pyrazole-5-carboxylate
https://huagongshe.com/reaction/1930343
Participants
| Role | Name | HCID | Charge |
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| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | HCID 66729263 | HCID 66729263 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | ethyl 3-tert-butyl-1-(2-(dimethylamino)ethyl)-1H-pyrazole-5-carboxylate | HCID 59588870 | 43% |
Reaction Steps
To a solution of ethyl 3-tert-butyl-1-(2-(dimethylamino)-2-oxoethyl)-1H-pyrazole-5-carboxylate (1.16 g, 4 mmol) in THF (10 mL) was added 1M borane/THF (12 ml, 12 mmol) at 0° C. under Ar and stirring continued for 12 h at 60° C. The mixture was cooled to 0° C., quenched with 3M HCl solution and heated to 60° C. for 30 min. The mixture was basified with solid NaHCO3 to pH around 8 and the product was extracted with CHCl3 (2×30 ml). The combined organics were washed with brine, dried (Na2SO4) and concentrated in vacuo provided crude product. Purification by silica gel chromatography provided ethyl 3-tert-butyl-1-(2-(dimethylamino)ethyl)-1H-pyrazole-5-carboxylate as a pasty mass (0.47 g, 43% yield). 1H NMR (400 MHz, MeOH-d4): δ 6.73 (s, 1H), 4.66 (t, J 6.8 Hz, 2H), 4.35 (q, J=7.2 Hz, 2H), 2.80 (t, J= 7.2 Hz, 2H), 2.34 (s, 6H), 1.38 (t, J=7.2 Hz, 3H), 1.31 (s, 9H); MS (ESI) m/z: 268.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08188113B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-f349f56e324e466fb140126ce2e1d9c8 |
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| Source note | uspto-grants-2012_05 |
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