HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1702693Erstellt: 26. Oktober 2026
1-Bromohexadecane → 4-Hexadecylaminobenzoylacetonitrile
https://huagongshe.com/reaction/1702693
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Bromohexadecane | HCID 8213 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Benzenepropanenitrile, 4-amino-beta-oxo- | HCID 96920 | — |
| Lösungsmittel | Hexamethylphosphoramide | HCID 12679 | — |
| Produkt | 4-Hexadecylaminobenzoylacetonitrile | HCID 20525834 | — |
Reaktionsschritte
A mixture of p-aminobenzoylacetonitrile, 1-bromohexadecane, potassium carbonate and hexamethylphosphoramide is heated to 80° C. for 20 hours and worked up as in Example 1, providing 4-hexadecylaminobenzoylacetonitrile. This material is dissolved in isopropanol and treated with an excess of sodium borohydride. After stirring at room temperature for 3 hours, the solution is concentrated, diluted with water and extracted with chloroform. The chloroform extract yields the crude carbinol which is heated to reflux for 1 hour with ethanol containing an equal volume of 2 N aqueous hydrochloric acid. The solution is then cooled, diluted with water and extracted with chloroform. The organic extract is washed successively with water and aqueous sodium bicarbonate, then dried and evaporated to afford 4-(hexadecylamino)cinnamonitrile.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04348399 |
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| Quelldatensatz | uspto-grants-1982_09 |
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| ORD ID | ord-6c0f44f169134eb7bf22eae09570c292 |
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| Quellennotiz | uspto-grants-1982_09 |
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