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HRID 220200Erstellt: 24. Oktober 2026

Picolinic acid → Diethyl 2-(5-bromopyridin-2-yl)malonate

https://huagongshe.com/de/reaction/220200

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPicolinic acidHCID 1018—
EduktDiethyl MalonateHCID 7761—
EduktCesium carbonateHCID 10796—
Edukt5-Bromo-2-iodopyridineHCID 593690—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktDiethyl 2-(5-bromopyridin-2-yl)malonateHCID 5923827050%

Reaktionsschritte

A mixture of 5-bromo-2-iodo-pyridine (56.8 g, 0.2 mol), malonic acid diethyl ester (64 g, 0.4 mol), CuI (3.8 g, 0.02 mol), Cs2CO3 (195.5 g, 0.6 mol) and pyridine-2-carboxylic acid (2.46 g, 0.04 mol) in 1,4-dioxane (400 mL) was stirred at 70 degrees Celsius under N2 for 24 hours. After cooling to room temperature, the solid was filtered and the solvent was evaporated. The residue was dissolved in ethyl acetate (400 mL) and washed with water, brine, dried over Na2SO4, filtered, concentrated in vacuo, the crude product was purified by flash chromatography (Petroleum Ether:EtOAc=20:1) to obtain an oil (31.6 g, 50%). MS: calc'd 316 (MH+), exp 316 (MH+). 1H NMR (d6-DMSO, 400 MHz), 8.68 (d, 1H, J=2.4 Hz), 8.11 (dd, 1H, J=2.4, 8.4 Hz), 7.45 (d, 1H, J=8.4 Hz), 5.16 (s, 1H), 4.20-4.07 (m, 4H), 1.18 (t, J=8.4 Hz, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202866B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-a0f0e68cae3740dab0a1c7d2c66551dc
Quellennotizuspto-grants-2012_06