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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243143Generated: November 3, 2026

2-Ethylbutyraldehyde → HCID 68593352, compound

https://huagongshe.com/reaction/2243143

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-EthylbutyraldehydeHCID 7359—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-BenzylimidazoleHCID 77918—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductHCID 68593352HCID 6859335269%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a chilled reaction vessel at −45° C. containing 1-benzyl-1H-imidazole (3.0 g, 19.0 mmol) in Et2O (100 mL) was added a solution of n-butyllithium (2.5M in hexanes, 10.8 mL, 26.9 mmol) dropwise. After 30 min, the reaction vessel was cooled to −78° C. and 2-ethylbutyraldehyde (2.8 mL, 22.8 mmol) was added dropwise. The reaction mixture was warmed to 0° C. and stirred for 15 min, then poured into sat. aqueous NH4Cl and extracted with Et2O. The organic layer was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The resulting yellow oil was purified by column chromatography (SiO2, EtOAc/hexane, 3:2, then 7:3) to yield a clear oil in 69% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674813B2
Source datasetuspto-grants-2010_03
ORD IDord-a44e7f27a04d4c39a6684a1d3272904f
Source noteuspto-grants-2010_03