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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1072481Erstellt: 27. Oktober 2026

Hydrochloric Acid → diethyl N,N'-[2-[[3,5-dichloro-4-[1-[5-(2-methylphenyl)-1,2,4-oxadiazol-3-yl]-1-methylethyl]phenyl]hydrazono]-1,3-dioxo-1,3-propanediyl]dicarbamate

https://huagongshe.com/reaction/1072481

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktCarbamic acid, (1,3-dioxo-1,3-propanediyl)bis-, diethyl esterHCID 154305—
EduktSodium AcetateHCID 517045—
Edukt3,5-Dichloro-4-[1-[5-(2-methylphenyl)-1,2,4-oxadiazol-3-yl]-1-methylethyl]benzenamineHCID 22386562—
EduktSodium NitriteHCID 23668193—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produktdiethyl N,N'-[2-[[3,5-dichloro-4-[1-[5-(2-methylphenyl)-1,2,4-oxadiazol-3-yl]-1-methylethyl]phenyl]hydrazono]-1,3-dioxo-1,3-propanediyl]dicarbamateHCID 22386569—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of intermediate (19) (0.0302 mole) and concentrated HCl (0.0906 mole) in acetic acid (100 ml) was stirred at 0° C. A solution of NaNO2 (0.032 mole) in water (10 ml) was added dropwise at 0° C. The reaction mixture was stirred for 1 hour at 0° C. A powdered mixture of sodium acetate (0.0906 mole) and diethyl(1,3-dioxo-1,3-propanediyl)biscarbamate (0.0332 mole) was added portionwise. The mixture was allowed to warm to RT and stirred for 1 hour. Water was added and this mixture was extracted with CH2Cl2. The separated organic layer was dried, filtered and the solvent evaporated, yielding diethyl N,N′-[2-[[3,5-dichloro-4-[1-[5-(2-methylphenyl)-1,2,4-oxadiazol-3-yl]-1-methylethyl]phenyl]hydrazono]-1,3-dioxo-1,3-propanediyl]dicarbamate (intermediate 20).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06911444B2
Quelldatensatzuspto-grants-2005_06
ORD IDord-d4518b950bac4db98bb4394c28151e1f
Quellennotizuspto-grants-2005_06