HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1781998Erstellt: 23. Oktober 2026
Dimethyl Sulfoxide → Benzyl 4-methylidenepiperidine-1-carboxylate
https://huagongshe.com/de/reaction/1781998
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Benzyl 4-oxopiperidine-1-carboxylate | HCID 643496 | — |
| Katalysator | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Produkt | Benzyl 4-methylidenepiperidine-1-carboxylate | HCID 15519136 | — |
Reaktionsschritte
A sodium hydride (13.2 g) was added to an anhydrous dimethylsulfoxide (176 mL) and the mixture was heated for 2 hours at 60° C. After cooling, to a suspension of methyltriphenylphosphonium bromide (110.4 g) in dimethylsulfoxide (120 mL) was added the reaction mixture, and the mixture was stirred for 30 minutes at room temperature. To the reaction mixture was added a solution of benzyl 4-oxo-1-piperidinecarboxylate (60 g) in dimethylsulfoxide (150 mL), the mixture was stirred for 1 hour at 50° C. After cooling, to the mixture was added water (2.5 L) and the mixture was extracted with ethyl acetate (1.5 L). The organic layer was washed with a saturated aqueous solution of ammonium chloride (0.5 L) and a saturated aqueous solution of sodium chloride (0.5 L), dried and then concentrated. The obtained residue was purified by column chromatography on silica gel (n-hexane:ethyl acetate:chloroform=9:1:1) to give the title compound (51.1 g) having the following physical data.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07498323B2 |
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| Quelldatensatz | uspto-grants-2009_03 |
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| ORD ID | ord-976196165fb343849eb72f934f0676e2 |
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| Quellennotiz | uspto-grants-2009_03 |
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