Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243127Generated: November 3, 2026

2-Ethylbutyraldehyde → HCID 68593443, compound

https://huagongshe.com/reaction/2243127

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-EthylbutyraldehydeHCID 7359—
ReactantEthyl AcetateHCID 8857—
Reactant1-(4-Methoxyphenyl)-1H-pyrazoleHCID 12238131—
ReactantButyllithiumHCID 178418339—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68593443HCID 6859344368%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674813B2
Source datasetuspto-grants-2010_03
ORD IDord-33d5001cbf5147f5b4d0f0593d8687c4
Source noteuspto-grants-2010_03