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HRID 1814731Erstellt: 25. Oktober 2026

Malononitrile → (+)-[[4-(3,6-dihydro-6-methyl-2-oxo-2H-1,3,4-thiadiazin-5-yl)phenyl]hydrazono]propanedinitrile

https://huagongshe.com/reaction/1814731

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMalononitrileHCID 8010—
EduktSodium AcetateHCID 517045—
Edukt5-(4-aminophenyl)-6-methyl-3H,6H-1,3,4-thiadiazine-2-oneHCID 22498613—
EduktSodium NitriteHCID 23668193—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelWaterHCID 962—
Lösungsmitteltert-ButanolHCID 6386—
Produkt(+)-[[4-(3,6-dihydro-6-methyl-2-oxo-2H-1,3,4-thiadiazin-5-yl)phenyl]hydrazono]propanedinitrileHCID 992625695%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

(+) 5-(4-aminophenyl)-6-methyl-3,6-dihydro-[1,3,4]-thiadiazin-2-one (1.34 g, 6 mmol) was dissolved in water (23 ml) and 6 N hydrochloric acid (4.5 ml). The solution was stirred and cooled. A cooled solution of sodiumnitrite (0.5 g) in water (5 ml) was added. Then a cooled solution of malononitrile (0.9 g) in t-butanol (54 ml) was added. In the end to the solution was added a cooled solution of sodium acetate (5.4 g) diluted in water (40 ml). The reaction mixture was stirred under cooling (0° C.) for 3 hours. After stirring the crystalline product was filtered and washed with water, yielding (+)-[[4-(3,6-dihydro-6-methyl-2-oxo-2H-1,3,4-thiadiazin-5-yl)phenyl]hydrazono]propanedinitrile as a crystalline solid (1.7 g) with optical purity of 100%, chromatografic purity 99.3%, m.p. 125-128° C., [a]D25=+1002°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06878702B2
Quelldatensatzuspto-grants-2005_04
ORD IDord-4c2ee9a6df964315988578e4e8473200
Quellennotizuspto-grants-2005_04