HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1285231Erstellt: 25. Oktober 2026
1,2-Diaminocyclohexane → 1,2-Diaminocyclohexane platinum (II) chloride
https://huagongshe.com/reaction/1285231
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,2-Diaminocyclohexane | HCID 4610 | — |
| Edukt | Potassium Chloride | HCID 4873 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Dipotassium tetrachloroplatinate | HCID 61440 | — |
| Edukt | Potassium hexachloroplatinate(IV) | HCID 61856 | — |
| Edukt | Hydrazinium chloride | HCID 115031 | — |
| Produkt | 1,2-Diaminocyclohexane platinum (II) chloride | HCID 426607 | 64% |
Reaktionsschritte
An 8 gram portion of platinum metal was digested in 250 ml of aqua regia to form chloroplatinic acid. Potassium chloride (12 g) solution was added to immediately precipitate potassium hexachloroplatinate(IV) which was subsequently reduced to potassium tetrachloroplatinite (II) with 2 grams of hydrazine hydrochloride. To the red aqueous solution of potassium tetrachloroplatinite was added 6 ml of 1,2-diaminocyclohexane (Aldrich) and enough 0.5N NaOH to adjust the pH to 7. After overnight stirring, 10 grams (64% yield) of dichloro(1,2-diaminocyclohexane)platinum was collected as a yellow precipitate. The commercial diaminocyclohexane used in this synthesis was a mixture of cis and trans isomers and the platinum complex was therefore also an isomeric mixture. It should be noted that isomerically pure complex can be prepared from readily synthesized cis and trans isomers of diaminocyclohexane or from easily resolved pure enantiomers thereof, as prepared by the process of, e.g., U.S. Pat. No. 4,169,846.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04565884 |
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| Quelldatensatz | uspto-grants-1986_01 |
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| ORD ID | ord-1f800714975b427280e16e9a9898bda9 |
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| Quellennotiz | uspto-grants-1986_01 |
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