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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805128Generated: November 2, 2026

HCID 68460100, compound → 6-Nitro-5-(trifluoromethyl)-1H-indole

https://huagongshe.com/reaction/1805128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68460100HCID 68460100—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
Product6-Nitro-5-(trifluoromethyl)-1H-indoleHCID 5931722531%

Reaction Conditions

Temperature135 °C

Reaction Steps

To a solution of 5-nitro-4-(trifluoromethyl)-2-((trimethylsilyl)ethynyl)aniline (6.0 g, 19.85 mmol) in DMF (30 mL) was added CuI (1.9 g, 9.976 mmol) under an atmosphere of nitrogen. The reaction mixture was heated at 135° C. in a sealed pressure flask overnight. The reaction mixture was then filtered and the filtrate was washed with water, dried over Na2SO4 and concentrated. The crude product was purified by silica gel column chromatography (5 to 20% EtOAc in petroleum as eluant) to obtain 6-nitro-5-(trifluoromethyl)-1H-indole (1.4 g, 31%). 1H NMR (400 MHz, CDCl3): δ 8.83 (br s, 1H), 8.15 (s, 1H), 8.11 (s, 1H), 7.58-7.57 (m, 1H), 6.80-6.79 (m, 1H); 19F NMR (282.4 MHz, CDCl3): δ-57.82; MS (ESI): m/z [M−H]− 229.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354427B2
Source datasetuspto-grants-2013_01
ORD IDord-9452f714329b47eb9a5f561bc020cb38
Source noteuspto-grants-2013_01