HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 483482Erstellt: 25. Oktober 2026
Water → N-(beta-n-butoxyacryloyl)-N-(1-benzyl-4-piperidinyl)aniline
https://huagongshe.com/reaction/483482
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | N-Phenyl-1-(phenylmethyl)-4-piperidinamine | HCID 70865 | — |
| Edukt | 3-Butoxyprop-2-enoyl chloride | HCID 53439772 | — |
| Lösungsmittel | Diisopropyl Ether | HCID 7914 | — |
| Produkt | N-(beta-n-butoxyacryloyl)-N-(1-benzyl-4-piperidinyl)aniline | HCID 54210636 | 98% |
Reaktionsschritte
To a mixture of N-(1-benzyl-4-piperidinyl)aniline (1.8 g), diisopropyl ether (20 ml) and triethylamine (0.87 g) is added dropwise a solution of β-n-butoxyacrylic acid chloride (1.4 g) in diisopropyl ether (5 ml) with stirring and heating at 70° C. After completion of dropwise addition, the mixture is further stirred with heating at the same temperature for 0.5 hour. After cooling, water is added to the reaction mixture and the mixture is subjected to extraction with ethyl acetate. The extract is washed with water and dried over magnesium sulfate. The solvent is distilled off under reduced pressure and the resulting residue is purified by silica gel column chromatography to give N-(β-n-butoxyacryloyl)-N-(1-benzyl-4-piperidinyl)-aniline (2.6 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05225402 |
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| Quelldatensatz | uspto-grants-1993_07 |
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| ORD ID | ord-961a585b2cfe4d859a4bab81ab32d461 |
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| Quellennotiz | uspto-grants-1993_07 |
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