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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963257Generated: October 30, 2026

Potassium Phosphate, Tribasic → (E)-Methyl 2-(4-fluorostyryl)isonicotinate

https://huagongshe.com/reaction/1963257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantMethyl 2-chloropyridine-4-carboxylateHCID 2736842—
Reactanttrans-2-(4-Fluorophenyl)vinylboronic acidHCID 5706776—
CatalystPalladium ChlorideHCID 24290—
Product(E)-Methyl 2-(4-fluorostyryl)isonicotinateHCID 6673205047.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

Methyl 2-chloroisonicotinate (5.5 g, 32.05 mmol), (E)-4-fluorostyrylboronic acid (7.98 g, 48.08 mmol), potassium phosphate (3.93 mL, 48.08 mmol) and PdCl2 (dppf) (0.464 g, 0.64 mmol) were split into 5 equal portions and each portion was placed in a microwave reaction vessel. The vessels were evacuated and backfilled with nitrogen. Methanol (15 mL) was added to each vessel, the vessels were sealed and heated in a single node microwave reactor at 100° C. for 10 min each. The contents of the vessels was pooled and water and DCM were added, the phases separated and the aqueous layer was extracted with DCM. The combined organic layers were filtered through a phase separator and evaporated. The residue was purified by automated flash chromatography on a Biotage® KP-SIL 340 g column. A gradient from 6:1 to 4:1 of EtOAc in heptane over 15 CV was used as mobile phase. (E)-Methyl 2-(4-fluorostyryl)isonicotinate (3.88 g, 47%) was isolated. 1H NMR (400 MHz, cdcl3) δ 3.98 (s, 3H), 7.04-7.18 (m, 3H), 7.52-7.62 (m, 2H), 7.63-7.71 (m, 2H), 7.93 (s, 1H), 8.74 (d, 1H). MS m/z 258 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-70c9b288aee14cb696c1a5193439166f
Source noteuspto-grants-2013_04