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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 250950Erstellt: 24. Oktober 2026

Sodium Carbonate → 3-p-Tolyl-pyridine-2-carbaldehyde

https://huagongshe.com/de/reaction/250950

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktTolylboronic acidHCID 79799—
Edukt3-Bromopyridine-2-carbaldehydeHCID 16414231—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTetrahydrofuran dimethoxyethaneHCID 22732251—
Produkt3-p-Tolyl-pyridine-2-carbaldehydeHCID 7723026677%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a stirred degassed solution of 3-bromo-2-pyridinecarboxaldehyde (198 mg, 1.06 mmol) and 4-methylbenzene boronic acid (152 mg, 1.12 mmol) in DME/THF (3.5 mL, 2.5:1) were added a 2 M Na2CO3 solution (0.9 mL) and Pd(PPh3)4 (63 mg, 0.055 mmol). The reaction mixture was flushed with Ar and maintained under Ar while being heated at 90° C. overnight. The mixture was then cooled and diluted with EtOAc (40 mL) and brine (30 mL). The organic layer was washed with brine (1×30 mL), dried (Na2SO4), filtered and concentrated. Purification of the resultant oil by column chromatography with silica gel (Hexanes/EtOAc, 2:1) afforded 3-p-tolyl-pyridine-2-carbaldehyde (161 mg, 77%) as a yellow oil. 1H NMR (CDCl3) δ 2.43 (s, 3H), 7.25-7.28 (m, 4H), 7.53 (dd, 1H, J=9, 6 Hz), 7.79 (dd, 1H, J=9, 1 Hz), 8.80 (dd, J=3, 1 Hz), 10.09 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07863293B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-4c5c936c45ed40f7af64fc58220f4daf
Quellennotizuspto-grants-2011_01