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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-5-nitro-2-(trifluoromethyl)pyridineHCID 22380051—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductEthyl-(5-nitro-2-trifluoromethyl-pyridin-4-yl)-amineHCID 22380174—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300945B2
Source datasetuspto-grants-2007_11
ORD IDord-2ecd0c3249354318bab9ad82c6f9f822
Source noteuspto-grants-2007_11