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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897767Generated: October 26, 2026

Sodium Carbonate → 2-Chloro-4-(5-formyl-pyridin-3-yl)-benzonitrile

https://huagongshe.com/reaction/1897767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant5-(Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carbaldehydeHCID 4992640—
Reactant4-Bromo-2-chlorobenzonitrileHCID 7010420—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product2-Chloro-4-(5-formyl-pyridin-3-yl)-benzonitrileHCID 59578397—

Reaction Steps

A mixture of 0.4-bromo-2-chlorobenzonitrile (1.082 g, 5 mmol), 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinaldehyde (1.165 g, 5.00 mmol), Pd(PPh3)4 (0.144 g, 0.125 mmol), sodium carbonate (2.5 mL, 5.00 mmol) in 1,4-dioxane (20 mL) was heated to reflux for 6 h. After cooling to room temperature, the solid was filtered and washed by ethyl acetate and water. After drying under vacuum, yellow powder was collected (1 g). 1H NMR (400 MHz, CDCl3): δ 7.63 (dd, J=1.68, 8 Hz, 1H), 7.79 (d, J=1.68 Hz, 1H), 7.83 (d, J=8 Hz, 1H), 8.35 (dd, J=2.24 Hz, 2.04 Hz, 1H), 9.07 (d, J=2.36 Hz, 1H), 9.15 (d, J=1.88 Hz, 1H), 10.22 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519142B2
Source datasetuspto-grants-2013_08
ORD IDord-aca8e19cc6dd4748b242c959b54fca71
Source noteuspto-grants-2013_08