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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432009Generated: October 30, 2026

Pyridine, 2-(trimethylstannyl)- → 3-Fluoro-5-(5-(2-pyridyl)-2-furyl)-benzonitrile

https://huagongshe.com/reaction/432009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine, 2-(trimethylstannyl)-HCID 11021057—
Reactant3-(5-Bromofuran-2-yl)-5-fluoro-benzonitrileHCID 21942457—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product3-Fluoro-5-(5-(2-pyridyl)-2-furyl)-benzonitrileHCID 2194249243.4%

Reaction Conditions

Temperature110 °C

Reaction Steps

Pd(PPh3)4 (10 mg, 0.009 mmol) was added to a solution of 3-(5-bromofuran-2-yl)-5-fluoro-benzonitrile (180 mg, 86% purity, 0.59 mmol) and 2-trimethylstannylpyridine (193 mg, 0.80 mmol) in toluene (2.5 mL) under argon. The resulting solution was stirred at 110° C. for 48 h. After cooling to room temperature, the solvent was removed in vacuo. Flash chromatography (silica gel, 35-100% dichloromethane in hexane) afforded 67.7 mg (43%) of 3-fluoro-5-(5-(2-pyridyl)-2-furyl)-benzonitrile. 1H-NMR (CDCl3), δ (ppm): 8.64 (d, 1H), 7.76-7.83 (m, 3H), 7.66 (m, 1H), 7.24 (m, 2H), 7.19 (d, 1H), 6.92 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660753B2
Source datasetuspto-grants-2003_12
ORD IDord-e03b379264b242f38f277f4a21d643f5
Source noteuspto-grants-2003_12