HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748074Generated: October 26, 2026
2-Ethylbutyraldehyde → 1-[1-(Benzyloxy)-1H-pyrazol-5-yl]-2-ethylbutan-1-ol
https://huagongshe.com/reaction/748074
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Ethylbutyraldehyde | HCID 7359 | — |
| Reactant | 1H-Pyrazole, 1-(phenylmethoxy)- | HCID 10058015 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[1-(Benzyloxy)-1H-pyrazol-5-yl]-2-ethylbutan-1-ol | HCID 68593374 | 72% |
Reaction Steps
To 1-benzyloxy-1H-pyrazole (prepared as described in JOC 60:4996 1995) dissolved in THF (20 mL) and cooled to −78° C. under a nitrogen atmosphere was added a solution of n-butyllithium (1.6 M in hexane, 2.0 mL, 3.2 mmol) via syringe over 10 min. After stirring at the above temperature for 1.25 h, 2-ethyl-butyraldehyde (0.42 mL, 3.4 mmol) was added dropwise. The mixture was then stirred at −78° C. for 1.5 h and quenched by dropwise addition of saturated aqueous ammonium chloride solution (3 mL). The mixture was warmed to ambient temperature and diluted with EtOAc, washed with saturated aqueous NaCl and the organic phase was dried over MgSO4. Filtration and evaporation of the organic extract produced an oil that was purified on a Biotage column (hexane/EtOAc, 6:1) to give the product as a clear colorless oil (0.565 g, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07399778B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-e4b8caaf70e24e7abd981bde71fb79a5 |
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| Source note | uspto-grants-2008_07 |
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