HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1704200Erstellt: 26. Oktober 2026
beta,beta'-Thiodipropionitrile → 3-cinnamoylamino-4-(2'-cyano-4',6'-dinitrophenylazo)-N,N-diethylaniline
https://huagongshe.com/reaction/1704200
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | beta,beta'-Thiodipropionitrile | HCID 8151 | — |
| Edukt | Sodium Cyanide | HCID 8929 | — |
| Edukt | 3-cinnamoylamino-4-(2'-bromo-4',6'-dinitrophenylazo)-N,N-diethylaniline | HCID 54057294 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 3-cinnamoylamino-4-(2'-cyano-4',6'-dinitrophenylazo)-N,N-diethylaniline | HCID 54527365 | 85,5% |
Reaktionsschritte
Into a solution composed of 6.8 parts of cuprous bromide in 300 parts by volume of bis-(β-cyanoethyl) sulfide, there are introduced 26 parts of 3-cinnamoylamino-4-(2'-bromo-4', 6'-dinitrophenylazo)-N,N-diethylaniline. The mixture is heated to 100° C. and, during several minutes, a solution of 2.6 parts of sodium cyanide in 16 parts of water is allowed to flow in. Stirring is continued for 1 to 2 hours more, at 115° C. After cooling to 30° C., the 3-cinnamoylamino-4-(2'-cyano-4',6'-dinitrophenylazo)-N,N-diethylaniline formed is separated, under the same conditions as in example 1. The yield is 85.5%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04126610 |
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| Quelldatensatz | uspto-grants-1978_11 |
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| ORD ID | ord-1875c55deca343338b28bab2887ad01d |
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| Quellennotiz | uspto-grants-1978_11 |
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