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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-EthylbutyraldehydeHCID 7359—
Reactant1H-Pyrazole, 1-(phenylmethoxy)-HCID 10058015—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-[1-(Benzyloxy)-1H-pyrazol-5-yl]-2-ethylbutan-1-olHCID 6859337472%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399778B2
Source datasetuspto-grants-2008_07
ORD IDord-e4b8caaf70e24e7abd981bde71fb79a5
Source noteuspto-grants-2008_07