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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 414210Erstellt: 24. Oktober 2026

Sulfuric Acid → 3,6-Dichloro-4-(1-ethyl-1-hydroxymethylpropyl)pyridazine

https://huagongshe.com/de/reaction/414210

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktPrenderolHCID 8284—
EduktAmmonium PersulfateHCID 62648—
Edukt3,6-DichloropyridazineHCID 67331—
KatalysatorSilver NitrateHCID 24470—
LösungsmittelWaterHCID 962—
Produkt3,6-Dichloro-4-(1-ethyl-1-hydroxymethylpropyl)pyridazineHCID 14349830—

Reaktionsschritte

Twenty g. of 3,6-dichloropyridazine, 2.3 g. of silver nitrate and 44.4 g. of 2,2-diethyl-1,3-propanediol were slurried in 280 ml. of water and 19.7 g. of sulfuric acid. To the mixture were added, simultaneously, solutions of 61.3 g. of ammonium persulfate in 200 ml. of water and 20 g. of silver nitrate in 40 ml. of water, over a period of 20 minutes at 55°. The mixture heated exothermically to 70°, and it was cooled to ambient temperature after the addition was complete. The aqueous layer was then decanted off, and the solids remaining were slurried twice in 800 ml. of diethyl ether. The resulting solution was shaken with the aqueous layer, and the layers were separated again. The aqueous layer was then made basic to pH 9 with ammonium hydroxide, and was re-extracted with 500 ml. of diethyl ether. The ether was evaporated under vacuum to obtain 46 g. of brown oil, which was purified by high performance liquid chromatography, eluting with 6:1 heptane:ethyl acetate. The product-containing fractions were combined and evaporated under vacuum to obtain, after recrystallization from diethyl ether/heptane, 0.54 g. of the desired product, m.p. 85°-87°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04791110
Quelldatensatzuspto-grants-1988_12
ORD IDord-b9ed69d905154ea89f39e0437edd28fd
Quellennotizuspto-grants-1988_12