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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2-Phenylindole | HCID 13698 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(Chloromethyl)-4-isobutoxybenzaldehyde | HCID 23157390 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-isobutoxy-3-[(2-phenyl-1H-indol-1-yl)methyl]benzaldehyde | HCID 23159929 | 36% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07517910B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-dad632bfc0054ae8a1a7ea8bed207ad3 |
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| Source note | uspto-grants-2009_04 |
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