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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 380728Erstellt: 27. Oktober 2026

Acetic Acid → (3,5-Dimethyl-4-nitropyridin-2-yl)methanol

https://huagongshe.com/reaction/380728

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktAcetic AnhydrideHCID 7918—
EduktSodium HydroxideHCID 14798—
Edukt4-Nitro-2,3,5-trimethylpyridine, 1-oxideHCID 11217611—
LösungsmittelMethanolHCID 887—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
Produkt(3,5-Dimethyl-4-nitropyridin-2-yl)methanolHCID 4049415—

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

151.3 gms (1.4833 mole) of acetic anhydride was added at 45-50° C. to a mixture of 90.0 gm (o.4595 moles) of 4-nitro-2,3,5-trimethylpyridine-N-oxide of formula-IV and 45.0 gms of acetic acid and heated to 85° C. and maintained at the temperature at 85-90° C. for 4 hrs. 75 ml of methanol was added to the reaction mixture at room temperature and distilled off acetic acid and methanol at temperature of 60-65° C. under vacuum to get an oil. 40% Sodium hydroxide solution (240 g) was added to the cooled oil at 0-5°°C. and stirred for 4 hrs. The crude product was obtained by extraction of the reaction mass with methylene chloride and distillation of the solvent. Pure 2-hydroxymethyl-3,5-dimethyl-4-nitropyridine of formula-II was obtained by re-crystallization of the crude material in toluene.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06303787B1
Quelldatensatzuspto-grants-2001_10
ORD IDord-414fc1153b5c4c07ba3f064f3d577a68
Quellennotizuspto-grants-2001_10