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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1755681Erstellt: 26. Oktober 2026

Formaldehyde → 3-(4-chlorophenylthio)-1-[N-(6-chloro-3-pyridylmethyl)-N-ethylamino]-1-methylamino-2-nitro-1-propene

https://huagongshe.com/reaction/1755681

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
Eduktp-ChlorothiophenolHCID 7815—
EduktN-((6-Chloro-3-pyridinyl)methyl)-N-ethyl-N'-methyl-2-nitro-1,1-ethenediamineHCID 86457—
LösungsmittelEthanolHCID 702—
Produkt3-(4-chlorophenylthio)-1-[N-(6-chloro-3-pyridylmethyl)-N-ethylamino]-1-methylamino-2-nitro-1-propeneHCID 8674882377,1%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

A mixture of 1-[N-(6-chloro-3-pyridylmethyl)-N-ethylamino]-1-methylamino-2-nitroethylene (2.71 g), p-chlorothiophenol (1.45 g), 37% aqueous solution of formaldehyde (0.97 g) and ethanol (30 ml) was stirred at 20° C. for 2 hours and under refluxing for 5 hours. The reaction mixture was concentrated and the residue was purified by column chromatography (eluting solvent:dichloromethane-methanol (6:1) to give 3-(4-chlorophenylthio)-1-[N-(6-chloro-3-pyridylmethyl)-N-ethylamino]-1-methylamino-2-nitro-1-propene (Compound No. 31) (3.30 g) as a yellow amorphous.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05438065
Quelldatensatzuspto-grants-1995_08
ORD IDord-2ee99acdce8e4a8e9a9440bc9ca4934b
Quellennotizuspto-grants-1995_08