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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621584Generated: November 2, 2026

Trifluoroacetic acid → 2-Fluoro-5-(1-(4-(methylthio)phenyl)vinyl)pyridine

https://huagongshe.com/reaction/1621584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(6-Fluoropyridin-3-yl)-1-(4-(methylthio)phenyl)ethanolHCID 66600361—
SolventDichloromethaneHCID 6344—
Product2-Fluoro-5-(1-(4-(methylthio)phenyl)vinyl)pyridineHCID 66600212100.7%

Reaction Steps

1-(6-Fluoropyridin-3-yl)-1-(4-(methylthio)phenyl)ethanol (1.261 g, 4.789 mmol) was dissolved in DCM (30 mL) and trifluoroacetic acid (1.0 mL, 13 mmol) was added, turning the solution dark green. The reaction was stirred at room temperature for 45 min and then was treated with saturated sodium bicarbonate (15 mL). The reaction was stirred for about 5 min, and then the layers were separated, and the aqueous phase was extracted with DCM. The organic phases were combined, dried over sodium sulfate, filtered, concentrated, and dried under high vacuum to give 2-fluoro-5-(1-(4-(methylthio)phenyl)vinyl)pyridine (1.183 g). 1H NMR (CDCl3, 400 MHz) δ 8.23 (d, J=2.35 Hz, 1H), 7.71 (td, J=8.12 Hz, 2.54 Hz, 1H), 7.26-7.21 (m, 4H), 6.91 (dd, J=8.51 Hz, 2.64 Hz, 1H), 5.55 (s, 1H), 5.43 (s, 1H), 2.51 (s, 3H). m/z (ESI, +ve ion) 246 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772480B2
Source datasetuspto-grants-2014_07
ORD IDord-3a19e3cab6634a95a010b4f62f6216d6
Source noteuspto-grants-2014_07