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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529652Generated: October 31, 2026

HCID 66676088, compound → 5-tert-butyl-6-nitro-1H-indole

https://huagongshe.com/reaction/1529652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66676088HCID 66676088—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
Product5-tert-butyl-6-nitro-1H-indoleHCID 5747020769%

Reaction Conditions

Temperature135 °C

Reaction Steps

To a solution of 4-tert-butyl-5-nitro-2-trimethylsilanylethynyl-phenylamine (25 g, 86 mmol) in DMF (100 mL) was added CuI (8.2 g, 43 mmol) under a nitrogen atmosphere. The mixture was heated at 135° C. in a sealed pressure flask overnight, cooled down to room temperature and filtered through a short plug of Celite. The filter cake was washed with EtOAc. The combined filtrate was washed with water, dried over Na2SO4 and concentrated. The crude product was purified by column chromatography (10-20% EtOAc/Hexane) to provide 5-tert-butyl-6-nitro-1H-indole as a yellow solid (12.9 g, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090619B2
Source datasetuspto-grants-2015_07
ORD IDord-5a97d1dcb5c34390866a5b1bf60d6d53
Source noteuspto-grants-2015_07