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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748043Generated: October 25, 2026

2-Ethylbutyraldehyde → 2-ethyl-1-{1-[(4-methylphenyl)sulfonyl]-1H-pyrazol-5-yl}butan-1-ol

https://huagongshe.com/reaction/748043

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-EthylbutyraldehydeHCID 7359—
Reactant1-TosylpyrozoleHCID 320750—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product2-ethyl-1-{1-[(4-methylphenyl)sulfonyl]-1H-pyrazol-5-yl}butan-1-olHCID 6859389675%

Reaction Steps

To 1-[(4-methylphenyl)sulfonyl]-1H-pyrazole (0.50 g, 2.26 mmol) [J. Chem. Res., Synopses, 10, 327 (1979)] in THF (23 mL) at −78° C. was added a solution of t-butyllithium (1.7 M in pentane, 1.5 mL, 2.49 mmol) dropwise. After 10 min 2-ethylbutyraldehyde (0.31 mL, 2.49 mmol) was added. After 10 min the reaction mixture was quenched with saturated aqueous ammonium chloride (5 mL) and then diluted with H2O (30 mL) and extracted with EtOAc (3×30 mL). The organic extract was dried (Na2SO4) and concentrated. The residue was purified by column chromatography (EtOAc/hexane, 3:7) to give 0.546 g (75%) of 2-ethyl-1-{1-[(4-methylphenyl)sulfonyl]-1H-pyrazol-5-yl}butan-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399778B2
Source datasetuspto-grants-2008_07
ORD IDord-d1886f497bab46c1aab4a1be25c8ce8f
Source noteuspto-grants-2008_07