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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1649046Erstellt: 25. Oktober 2026

Methyl fluorosulfate → N-(3-methyl-2-oxazolidinylidene)-N'-phenyl-1-pyrrolidinecarboximidamide fumarate

https://huagongshe.com/reaction/1649046

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl fluorosulfateHCID 9870—
EduktSodium HydroxideHCID 14798—
Edukt2-Oxazolidinone, 3-methyl-HCID 29831—
EduktFumaric AcidHCID 444972—
EduktHCID 178511988HCID 178511988—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(3-methyl-2-oxazolidinylidene)-N'-phenyl-1-pyrrolidinecarboximidamide fumarateHCID 70510611—

Reaktionsschritte

To a solution of 3-methyloxazolidin-2-one, 2.02 g (0.02 mole), in dry methylene chloride under dry nitrogen is added 2.28 g (0.02 mole) of methyl fluorosulfonate in one portion. After stirring 3 hrs, 0.02 mole of N-phenyl-1-pyrrolidinecarboximidamide free base in dry methylene chloride is added. After stirring at room temperature overnight, the solution is shaken with excess cold 3 N NaOH. The organic layer is separated and dried over K2CO3, filtered, and the solvent removed in vacuo to afford the crude base. Addition of an equimolar amount of fumaric acid to a solution of the free base in isopropanol, followed by recrystallization from isopropanol/ether affords pure N-(3-methyl-2-oxazolidinylidene)-N'-phenyl-1-pyrrolidinecarboximidamide fumarate; m.p. 160°-162° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04414211
Quelldatensatzuspto-grants-1983_11
ORD IDord-e962d691496846a3a53882cbbe5133fd
Quellennotizuspto-grants-1983_11