HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243127Generated: November 3, 2026
2-Ethylbutyraldehyde → HCID 68593443, compound
https://huagongshe.com/reaction/2243127
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Ethylbutyraldehyde | HCID 7359 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-(4-Methoxyphenyl)-1H-pyrazole | HCID 12238131 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68593443 | HCID 68593443 | 68% |
Reaction Steps
To a chilled reaction vessel at −78° C. containing 1-(4-methoxyphenyl)-1H-pyrazole (Tetrahedron Lett. 39(19), 2941-2944, (1998)) (1.096 g, 6.3 mmol) in THF (40 mL) was added a solution of n-butyllithium (2.5M in hexanes, 2.5 mL, 6.4 mmol) dropwise and the mixture was stirred for 1 h. 2-Ethylbutyraldehyde (0.93 mL, 7.5 mmol) was then added dropwise and, after 15 min, the reaction mixture was warmed to room temperature and stirred for 18 h. The reaction mixture was diluted with 0.1N HCl and stirred for 15 min, then poured into a separatory funnel containing EtOAc. The organic layer was separated, dried over MgSO4, filtered and concentrated in vacuo. The resulting oil was purified by column chromatography (SiO2, EtOAc/hexane, 1:4) to yield a pure oil in 68% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674813B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-33d5001cbf5147f5b4d0f0593d8687c4 |
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| Source note | uspto-grants-2010_03 |
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