HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1032000Erstellt: 25. Oktober 2026
Benzaldehyde → Bis(4-(2-benzalaminoethyl)piperazine-1-thiocarbonyl) Disulfane
https://huagongshe.com/reaction/1032000
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzaldehyde | HCID 240 | — |
| Edukt | Carbon Disulfide | HCID 6348 | — |
| Edukt | Aminoethylpiperazine | HCID 8795 | — |
| Katalysator | Potassium ferricyanide | HCID 26250 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | Bis(4-(2-benzalaminoethyl)piperazine-1-thiocarbonyl) Disulfane | HCID 86744207 | — |
Reaktionsschritte
10.6 parts of benzaldehyde are added to a solution of 12.9 parts of 1-(2-aminoethyl)piperazine in 24 parts of water and 24 parts of ethanol. 7.6 parts of carbon disulfide are then slowly added dropwise with ice cooling, whereby a precipitate forms. This is again dissolved after dilution with 100 parts each of water and of ethanol by addition of 10.1 parts of triethylamine and oxidized with 33 parts with potassium hexacyanoferrate(III). The product that now precipitates is filtered, washed repeatedly with water and finally with methanol, and dried at 30° C. in vacuum. Obtained are 26 parts of a substance with 56.4% C, 6.3% H, 14.5% N, and 21.5% S (calculated: 57.5% C, 6.2% H, 14.4% N, 21.9% S), which corresponds to the title compound of this Example according to IR and 1H-NMR.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04956433 |
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| Quelldatensatz | uspto-grants-1990_09 |
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| ORD ID | ord-d248eaf8c8f946bf876c71d1d6e3a01d |
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| Quellennotiz | uspto-grants-1990_09 |
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