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HRID 647793Erstellt: 24. Oktober 2026

Methomyl → Methyl N-[[[[[(5,5-dimethyl-2-thioxo-1,3,2-dioxaphosphorinan-2-yl)(methyl)amino]sulfinyl]methylamino]carbonyl]oxy]ethanimidothioate

https://huagongshe.com/de/reaction/647793

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethomylHCID 4109—
EduktThionyl ChlorideHCID 24386—
Edukt5,5-Dimethyl-2-(methylamino)-1,3,2lambda~5~-dioxaphosphinane-2-thioneHCID 254964—
LösungsmittelPyridineHCID 1049—
ProduktMethyl N-[[[[[(5,5-dimethyl-2-thioxo-1,3,2-dioxaphosphorinan-2-yl)(methyl)amino]sulfinyl]methylamino]carbonyl]oxy]ethanimidothioateHCID 86739078—

Reaktionsschritte

Methyl N-[[[[[(5,5-dimethyl-2-thioxo-1,3,2-dioxaphosphorinan-2-yl)(methyl)amino]sulfinyl]methylamino]carbonyl]oxy]ethanimidothioate was prepared by the procedure employed in Example 9, by reacting methyl N-[[(methylamino)carbonyl]oxy]ethanimidothioate (2.43 g, 0.015 mole), thionyl chloride (1.79 g, 0.015 mole), and 5,5-dimethyl-2-methylamino-2-thioxo-1,3,2-dioxaphosphorinan (2.93 g, 0.015 mole) in pyridine (10 ml). Recrystallization from chloroform-hexane afforded 3.0 g of needles of the formula below, mp 112~114°. ##STR33##

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04410518
Quelldatensatzuspto-grants-1983_10
ORD IDord-9565aca774ea492c939ef665622c8f8d
Quellennotizuspto-grants-1983_10