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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 619875Erstellt: 26. Oktober 2026

Nitric Acid → 2-Chloro-4-nitropyridine 1-oxide

https://huagongshe.com/reaction/619875

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitric AcidHCID 944—
EduktSulfuric AcidHCID 1118—
Edukt2-Chloropyridine oxideHCID 75465—
Produkt2-Chloro-4-nitropyridine 1-oxideHCID 84433—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

With stirring, 1.5 liters of concentrated sulfuric acid was cooled to 0° C. and 1058 grams (6.06 moles) of 2-chloropyridine-N oxide was added portionwise during a 5 hour period. The reaction mixture temperature was maintained at 5°-10° C. and 590 ml of 90% nitric acid was added dropwise. Upon completion of addition the reaction mixture was heated to 80° C. and the source of heat was removed. The exothermic reaction caused the reaction mixture temperature to rise to 115° C. During a one hour period the reaction mixture temperature fell from 115° C. to 100° C., where it was maintained for four hours with an external heat source. The reaction mixture was cooled then poured into 12 liters of ice. The resultant solid was collected by filtration and washed three times by suspension in three one-liter portions of water. The solid was dried to yield 715 grams of 2-chloro-4-nitropyridine-N oxide. The mother liquor and washes were combined and extracted with four one-liter portions of chloroform. The combined extracts were dried with potassium carbonate and filtered. The filtrate was concentrated under under reduced pressure to a residual solid. The solid was triturated in 65 ml of 2-propanol to yield an additional 94.2 grams of 2-chloro-4-nitropyridine-N oxide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04818271
Quelldatensatzuspto-grants-1989_04
ORD IDord-51982e60977c4796b9654cdc758ba9d8
Quellennotizuspto-grants-1989_04