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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110851Generated: November 4, 2026

Sodium Iodide → 4-isobutoxy-3-[(2-phenyl-1H-indol-1-yl)methyl]benzaldehyde

https://huagongshe.com/reaction/2110851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant2-PhenylindoleHCID 13698—
ReactantSodium hydrideHCID 24758—
Reactant3-(Chloromethyl)-4-isobutoxybenzaldehydeHCID 23157390—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-isobutoxy-3-[(2-phenyl-1H-indol-1-yl)methyl]benzaldehydeHCID 2315992936%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-phenyl-1H-indole (0.94 g, 4.85 mmol) in N,N-dimethylformamide (10 mL) was added sodium hydride (60% in oil, 0.19 g, 4.85 mmol) with stirring at 0° C., and the mixture was stirred at the same temperature for 5 min. 3-(Chloromethyl)-4-isobutoxybenzaldehyde (1.0 g, 4.41 mmol) and sodium iodide (0.73 g, 4.85 mmol) were added to the obtained mixture and the mixture was stirred at the same temperature for 2 hr. After completion of the reaction, the reaction mixture was diluted with ethyl acetate, and the mixture was washed with 5% aqueous potassium hydrogensulfate solution and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-hexane/ethyl acetate=4/1) to give the title compound (0.60 g, yield 36%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517910B2
Source datasetuspto-grants-2009_04
ORD IDord-dad632bfc0054ae8a1a7ea8bed207ad3
Source noteuspto-grants-2009_04