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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455196Generated: November 1, 2026

2-Chloro-3-(trifluoromethyl)pyridine → 2-Ethoxy-3-(trifluoromethyl)pyridine

https://huagongshe.com/reaction/1455196

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-3-(trifluoromethyl)pyridineHCID 589833—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
Product2-Ethoxy-3-(trifluoromethyl)pyridineHCID 42632356—

Reaction Steps

2-Chloro-3-trifluoromethyl-pyridine (4.43 g, 24.4 mmol) was dissolved in 42 ml 21% (wt.) sodium ethoxide in ethanol. The mixture was stirred at ambient temperature for 1.5 days. After this period of time, the solvent was evaporated and the residue was taken into water and extracted with dichloromethane three times. The combined extract was washed with brine, dried over sodium sulfate, and concentrated in vacuo to give 2-ethoxy-3-trifluoromethyl-pyridine as a light liquid (3.42 g, 73% yield). The crude product was used directly for the next step. 1H-NMR (400 MHz, CDCl3): δ 1.42 (t, 3H, J=7.07), 4.49 (q, 2H, J=7.07), 6.94 (dd, 1H, J=7.45, J=5.05), 7.85 (dd, 1H, J=1.26, J=7.45), 8.30 (dd, 1H, J=1.26, J=5.06).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482366B2
Source datasetuspto-grants-2009_01
ORD IDord-7a2d696038eb432a998cb31ec916b264
Source noteuspto-grants-2009_01