HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404867Generated: November 1, 2026
HCID 68460100, compound → 6-Nitro-5-(trifluoromethyl)-1H-indole
https://huagongshe.com/reaction/2404867
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 68460100 | HCID 68460100 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Nitro-5-(trifluoromethyl)-1H-indole | HCID 59317225 | 31% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802700B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-50b0409d0dc14a06a0ffb85baeffabd9 |
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| Source note | uspto-grants-2014_08 |
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