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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908434Generated: October 28, 2026

Tetrabutylammonium Fluoride → 2-Tert-butyl-5-nitro-1H-indole-7-carbonitrile

https://huagongshe.com/reaction/1908434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant2-Amino-3-(3,3-dimethylbut-1-ynyl)-5-nitrobenzonitrileHCID 59129252—
SolventTetrahydrofuranHCID 8028—
Product2-Tert-butyl-5-nitro-1H-indole-7-carbonitrileHCID 5342118451.1%

Reaction Steps

To a solution of 2-amino-3-(3,3-dimethylbut-1-ynyl)-5-nitrobenzonitrile (1.7 g, 7.0 mmol) in THF (35 mL) was added TBAF (9.5 g, 28 mmol) at room temperature. The mixture was heated at reflux overnight. The reaction mixture was cooled and the THF was removed under reduced pressure. Water (50 ml) was added to the residue and the mixture was extracted with EtOAc. The organics were dried over Na2SO4 and the solvent was evaporated under vacuum to obtain 0.87 g of crude product 2-tert-butyl-5-nitro-1H-indole-7-carbonitrile which was used directly in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598181B2
Source datasetuspto-grants-2013_12
ORD IDord-438cbe7e3b244385970067a77042cbb1
Source noteuspto-grants-2013_12