HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666871Generated: October 30, 2026
Sodium Hydroxide → 2-(5-(trifluoromethyl)-1H-indol-3-yl)ethanamine
https://huagongshe.com/reaction/1666871
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 2-(5-(trifluoromethyl)-1H-indol-3-yl)-2-oxo-acetamide | HCID 21071424 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(5-(trifluoromethyl)-1H-indol-3-yl)ethanamine | HCID 12030136 | — |
Reaction Steps
Add LiAlH4 (37.95 g, 1.00 mol) to THF (650 mL) under ice-bath cooling. Prepare a solution of AlCl3 (50 g, 375 mmol) in THF (600 ml) and add dropwise to the LiAlH4 solution over 45 min at 5-1° C. While maintaining the temperature at about 5° C., add a solution of 2-(5-(trifluoromethyl)-1H-indol-3-yl)-2-oxo-acetamide (21.4 g, 83.5 mmol) in THF (600 ml) and stir overnight with warning to ambient temperature. Cool the mixture with ice water and treat with 30% NaOH (100 ml) while maintaining the temperature at less than about 30° C. After stirring for about 30 minutes, filter, wash with THF (2 L), and evaporate the filtrate to give the title compound. Form of the HCl salt by dissolving the title compound in diethyl ether and adding of a solution of HCl in diethyl ether (until acidic). Collect the solid by filtration, wash with diethyl ether, and dry under reduced pressure to give the hydrochloride salt of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044090B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-d913e9b96aec4c63b59e12884642049c |
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| Source note | uspto-grants-2011_10 |
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