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HRID 1924821Erstellt: 24. Oktober 2026

2-Chloro-6-methylpyridine-4-carboxylic acid → 2-Chloro-6-methyl-isonicotinic acid tert-butyl ester

https://huagongshe.com/de/reaction/1924821

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloro-6-methylpyridine-4-carboxylic acidHCID 141209—
Edukt1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamineHCID 547712—
LösungsmittelTolueneHCID 1140—
Produkt2-Chloro-6-methyl-isonicotinic acid tert-butyl esterHCID 86040366—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

N,N-dimethylformamide-di-tert.-butyl-acetal (19 mL, 80 mmol) is added during 40 min to a hot (65° C., flask temperature) suspension of 2-chloro-6-methyl-isonicotinic acid (3.40 g, 19.8 mmol) in dry toluene (100 mL). The clear orange solution is stirred at 80° C. for 48 h, cooled to rt and diluted with toluene (100 mL). The solution is washed with water (2×40 mL), sat. aq. NaHCO3 (3×30 mL) and sat. aq. NaCl (25 mL), dried (Na2SO4), filtered and evaporated. The residue is purified by FC (SiO2, DCM-MeOH) to give 2-chloro-6-methyl-isonicotinic acid tert-butyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08178562B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-ddf186e5a9d84329b922b4a73876dabe
Quellennotizuspto-grants-2012_05