Synthesis method for copper octoate
A synthesis method, copper octoate technology, applied in the separation/purification of carboxylic acid compounds, carboxylate preparation, organic chemistry, etc., can solve the problems of packaging, complicated preparation methods, and reducing the purity of copper octoate
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[0031] The embodiment of the present application provides a kind of synthetic method of copper octanoate, it comprises the following steps:
[0032] Step S1: mixing n-octanoic acid, copper oxide and a solvent, dissolving n-octanoic acid in the solvent, and reacting at a temperature higher than the boiling point of the solvent to obtain a reactant.
[0033] The reaction equation of above-mentioned reaction is as follows:
[0034] 2C 7 h 15 COOH+CuO=(C 7 h 15 COO) 2 Cu+H 2 O.
[0035] It should be noted that octanoic acid in this example is straight-chain n-octanoic acid, and copper n-octanoate refers to straight-chain n-octanoic acid copper; usually, if iso-octanoic acid is used as a raw material, n-octoate copper cannot be obtained.
[0036] In order to ensure that the reaction is carried out completely, while avoiding the introduction of difficult-to-remove impurities, the molar ratio of n-octanoic acid to copper oxide is 0.1-2:1, and the molar ratio of n-octanoic acid...
Embodiment 1
[0053] The present embodiment provides a kind of copper octanoate product, and its synthesis route is as follows:
[0054] Take by weighing 24.8g copper oxide powder, place in the round bottom flask of 1L, add 22.5g n-octanoic acid, (the molar ratio of n-octanoic acid and copper oxide is 0.5:1) add 500mL dehydrated alcohol again, stir, let n-octanoic acid fully Dissolve in absolute ethanol.
[0055] Place the round-bottomed flask in a water bath, install a condenser tube and feed condensed water, control the temperature of the water bath at 90°C, and fully reflux the reaction for 36 hours. After the mixture of n-octanoic acid and absolute ethanol gradually turns dark green, the reaction product is obtained. .
[0056] The reactant was centrifuged to obtain the liquid fraction.
[0057] The liquid components were slowly evaporated to dryness, the evaporation temperature was 80° C., and the evaporation time was 3 hours to obtain solid components.
[0058] Vacuum-dry the obtai...
Embodiment 2
[0061] This embodiment provides a kind of copper octoate product, and its synthesis route is basically the same as the synthesis route of embodiment 1, and difference is:
[0062] Take by weighing 12.4g copper oxide powder, place in the round bottom flask of 1L, add 22.5g n-octanoic acid, (the mol ratio of n-octanoic acid and copper oxide is 1:1) add 500mL dehydrated alcohol again, stir, let n-octanoic acid fully Dissolved in absolute ethanol to finally obtain copper octoate product.
[0063] After testing, the copper octoate purity of the copper octoate product is 99.3%, and the yield is 90.3%.
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