HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594094Generated: October 30, 2026
Ethylamine → Ethyl-(5-nitro-2-trifluoromethyl-pyridin-4-yl)-amine
https://huagongshe.com/reaction/1594094
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chloro-5-nitro-2-(trifluoromethyl)pyridine | HCID 22380051 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl-(5-nitro-2-trifluoromethyl-pyridin-4-yl)-amine | HCID 22380174 | — |
Reaction Steps
K2CO3 (4.15 g, 30.01 mmol), and 2.0 M solution of EtNH2 (15 mL, 30.01 mmol) in THF are added o a solution of 4-chloro-5-nitro-2-trifluoromethyl-pyridine (3.4 g, 15.0 mmol) in acetonitrile (30 mL) under cold conditions. The reaction is complete after stirring at 0° C. for 2 h. Usual work up affords ethyl-(5-nitro-2-trifluoromethyl-pyridin-4-yl)-amine as an yellow-orange viscous oil. 1H NMR (300 MHz, CDCl3): δ 9.24 (s, 1H), 7.09 (s, 1H), 3.45 (t, J=7.2 Hz, 2H), 1.42 (t, J=7.2 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07300945B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-2ecd0c3249354318bab9ad82c6f9f822 |
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| Source note | uspto-grants-2007_11 |
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