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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl fluorosulfate | HCID 9870 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2-Oxazolidinone, 3-methyl- | HCID 29831 | — |
| Edukt | Fumaric Acid | HCID 444972 | — |
| Edukt | HCID 178511988 | HCID 178511988 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-(3-methyl-2-oxazolidinylidene)-N'-phenyl-1-pyrrolidinecarboximidamide fumarate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04414211 |
|---|
| Quelldatensatz | uspto-grants-1983_11 |
|---|
| ORD ID | ord-e962d691496846a3a53882cbbe5133fd |
|---|
| Quellennotiz | uspto-grants-1983_11 |
|---|