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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1366822Erstellt: 26. Oktober 2026

Water → 3-Bromo-6-acetamidopyridine-2-carboxylic acid

https://huagongshe.com/reaction/1366822

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium CarbonateHCID 11430—
EduktPotassium PermanganateHCID 516875—
Edukt2-Acetamido-5-bromo-6-methylpyridineHCID 954589—
LösungsmittelPyridineHCID 1049—
Produkt3-Bromo-6-acetamidopyridine-2-carboxylic acidHCID 25306988603,8%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a solution of N-(5-bromo-6-methyl-pyridin-2-yl)-acetamide 48.46 g in pyridine 250 ml was added water 250 ml and the mixture warmed to 90° C. and potassium carbonate 2.2 g was added. Potassium permanganate was added portionwise over 10 h and the mixture allowed to cool slowly overnight. The reaction mixture was re-heated to 90° C. for 2 h, cooled slightly and filtered to remove manganese dioxide. The filtrate was evaporated in vacuo and the residue partitioned between water 1 L and ethyl acetate 500 ml. The aqueous solution was washed with ethyl acetate. The organic solutions were combined, washed with brine, dried MgSO4 and evaporated in vacuo to recover unchanged starting materials 12.6 g. The aqueous solution was acidified with concentrated hydrochloric acid (circa 80 ml) and the solid product filtered off, washed with a minimum of water, sucked dry and then dried at 80° C. (vac) to give 6-acetylamino-3-bromo-pyridine-2-carboxylic acid 24.9 g

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07893077B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-f06965780ec74d4d9f5a69f09679b26e
Quellennotizuspto-grants-2011_02