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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285231Generated: October 25, 2026

1,2-Diaminocyclohexane → 1,2-Diaminocyclohexane platinum (II) chloride

https://huagongshe.com/reaction/1285231

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DiaminocyclohexaneHCID 4610—
ReactantPotassium ChlorideHCID 4873—
ReactantSodium HydroxideHCID 14798—
ReactantDipotassium tetrachloroplatinateHCID 61440—
ReactantPotassium hexachloroplatinate(IV)HCID 61856—
ReactantHydrazinium chlorideHCID 115031—
Product1,2-Diaminocyclohexane platinum (II) chlorideHCID 42660764%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04565884
Source datasetuspto-grants-1986_01
ORD IDord-1f800714975b427280e16e9a9898bda9
Source noteuspto-grants-1986_01