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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802825Generated: November 2, 2026

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

https://huagongshe.com/reaction/1802825

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) obtained in Step 2 was dissolved in tetrahydrofurane (30 mL), and 1 M tetrabutylammoniumfluoride solution (5.2 mL, 5.2 mmol) was added in drops at 0° C. At the end of reaction, the resulting mixture was diluted with water and extracted with ethylacetate. The extract was washed with saturated sodium chloride solution, dried over anhydrous magnesium sulfate and filtered. The solvent was removed under reduced pressure and the residue was separated using column chromatography to give 5-chloro-3-phenyl-7-nitro-1H-indole (1.2 g, Yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349885B2
Source datasetuspto-grants-2013_01
ORD IDord-4599e6e4bc7f485781140124c9c69bd3
Source noteuspto-grants-2013_01