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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466477Generated: October 31, 2026

Tetrabutylammonium Fluoride → 5-Chloro-3-phenyl-7-nitro-1H-indole

https://huagongshe.com/reaction/1466477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant5-Chloro-7-nitro-3-phenyl-2-trimethylsilyl-1H-indoleHCID 68476076—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-3-phenyl-7-nitro-1H-indoleHCID 68471840101.2%

Reaction Steps

5-Chloro-7-nitro-3-phenyl-2-trimethylsilyl-1H-indole (1.5 g, 4.35 mmol) prepared in Step A was dissolved in tetrahydrofuran (30 mL), and tetrabutylammonium fluoride 1M solution (5.2 mL, 5.2 mmol) was added in drops thereto at 0° C. After completion of the reaction, the reaction mixture was diluted with water, extracted with ethyl acetate, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (1.2 g, Yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000028B2
Source datasetuspto-grants-2015_04
ORD IDord-026cdf792ce2417ebb470507961ab73f
Source noteuspto-grants-2015_04