Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Thioacetic acid | HCID 10484 | — |
| Edukt | HCID 18642546 | HCID 18642546 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 18642555 | HCID 18642555 | — |
Reaktionsschritte
A solution of (2S,4R)-2-(2-fluoroethyloxymethyl)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (4.95 g) in dimethylformamide (5 ml) was added to a mixture of thioacetic S-acid (1.26 ml) and potassium tert-butoxide (1.98 g) in dimethylformamide (25 ml) in a nitrogen stream, and the mixture was heated at 75°-80° C. for 2 hours. The mixture was poured into ice-water (100 ml) and extracted with ethyl acetate (100 ml). The extract was washed with water (100 ml×2) and brine (100 ml), in turn, dried over magnesium sulfate, and concentrated under reduced pressure to give a syrup. The syrup was subjected to a column chromatography on silica gel (80 g) and eluted with chloroform to give (2S,4S)-4-acetylthio-2-(2-fluoroethyloxymethyl)-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (1.75 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04983596 |
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| Quelldatensatz | uspto-grants-1991_01 |
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| ORD ID | ord-561050ac5e184cdba136ada41a18f756 |
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| Quellennotiz | uspto-grants-1991_01 |
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