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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 457550Erstellt: 24. Oktober 2026

2-Methyl-2-butene → 4-Iodo-2-methoxypyridine-3-carboxylic acid

https://huagongshe.com/de/reaction/457550

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Methyl-2-buteneHCID 10553—
Edukt4-Iodo-2-methoxynicotinaldehydeHCID 10038381—
EduktSodium ChloriteHCID 23668197—
EduktMonosodium phosphateHCID 23672064—
LösungsmittelFormic AcidHCID 284—
LösungsmittelWaterHCID 962—
Lösungsmitteltert-ButanolHCID 6386—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Iodo-2-methoxypyridine-3-carboxylic acidHCID 1843994067%

Reaktionsschritte

To a solution of 4-iodo-2-methoxy-pyridine-3-carbaldehyde (4.96 g, 18.9 mmol) in 22 mL tert.-butanol was added in this order 2-methyl-2-butene (30 mL of a 2 M solution in THF, 60 mmol), natriumdihydrogen-phosphate (5.7 g, 47.5 mmol), water (15 mL) and sodiumchlorite (3.9 g, 43 mmol). The mixture was stirred at ambient temperature for 1 hour, then poured on dilute aqueous formic acid. The mixture was extracted with ethyl acetate, the organic layer washed with water and brine and concentrated. The residue was dissolved in diisopropylether+dichloromethane (1+1) and extracted 3 times with half-concentrated aqueous NaOH solution. The combined aqueous layers were acidified with conc. HCl and extracted with ethyl acetate. The organic layers were washed with water and brine, then dried over sodium sulfate and concentrated to give 3.462 g of the title compound as a white solid (67%). 1H NMR (500 MHz, CD3OD) δ 7.83 (d, J=5.4 Hz, 1H), 7.43 (d, J=5.4 Hz, 1H), 3.94 (s, 3H);

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07189716B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-95f44250f2ae4abf80b18a4681f20a35
Quellennotizuspto-grants-2007_03