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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404592Generated: October 30, 2026

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

https://huagongshe.com/reaction/404592

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 5747020768.7%

Reaction Conditions

Temperature135 °C

Reaction Steps

To a solution of 4-tert-butyl-5-nitro-2-trimethylsilanylethynylphenylamine (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 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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748612B2
Source datasetuspto-grants-2014_06
ORD IDord-59e7625e977d4281bb8077700a5bdfc1
Source noteuspto-grants-2014_06