HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1171657Erstellt: 25. Oktober 2026
Ammonium Chloride → (E)-3-[(Pyrrol-2-yl)methylidene]-1-(triphenylmethyl)piperidin-4-one
https://huagongshe.com/reaction/1171657
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 1-Tritylpiperidin-4-one | HCID 2748414 | — |
| Edukt | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Edukt | tert-Butyl 2-formyl-1H-pyrrole-1-carboxylate | HCID 5057005 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (E)-3-[(Pyrrol-2-yl)methylidene]-1-(triphenylmethyl)piperidin-4-one | HCID 23138769 | 35% |
Reaktionsschritte
To a solution of 1-(triphenylmethyl)piperidin-4-one (17.00 g) in tetrahydrofuran (400 ml) was added dropwise a 0.5N solution of potassium bis(trimethylsilyl)amide in toluene (100 ml) at −70° C., and the resulting mixture was stirred at the same temperature for 20 minutes. Subsequently, to the reaction mixture was added dropwise a solution of 1-(t-butoxycarbonyl)pyrrole-2-carbaldehyde (11.00 g) in tetrahydrofuran (100 ml) at −70° C., and the resulting mixture was stirred at the same temperature for 1 hour. After saturated aqueous ammonium chloride solution was added, the resulting reaction mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium chloride solution and the organic layer was dried over anhydrous magnesium sulfate. The solvent was removed in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate, hexane, and dichloromethane (1:3:1) as the eluent to afford the title compound (7.26 g, yield: 35%) as a yellow amorphous solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07829580B2 |
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| Quelldatensatz | uspto-grants-2010_11 |
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| ORD ID | ord-c8197e42b60344b9ba78b7da8b756cb7 |
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| Quellennotiz | uspto-grants-2010_11 |
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