![](/CAS/GIF/2915-53-9.gif)
Dioctyl maleate synthesis
- Product Name:Dioctyl maleate
- CAS Number:2915-53-9
- Molecular formula:C20H36O4
- Molecular Weight:340.5
Yield:-
Reaction Conditions:
with potassium hydroxide in chloroform;1-bromo-hexane;water;Petroleum ether
Steps:
2.ii (ii)
(ii) Preparation of Hexyl/Octyl Maleate/Fumarate Monooctyl maleic/fumaric acid (88 g, 0.39 mole) was dissolved in chloroform (200 ml) and was stirred in a 1 L Erlenmeyer (Quick Fit) flask, fitted with condenser, with a solution of potassium hydroxide (21 g, 0.38 mole) and tetrabutyl ammonium iodide (15 g, 0.04 mole) in 200 mls of water. To the stirred mixture was added hexyl bromide 64 g, 0.39 mole) and the two phase mixture was stirred rapidly under reflux for 5 hours. The chloroform layer was separated off, washed with sodium carbonate solution, then with water, and then dried over sodium sulphate. After filtering and evaporating the resulting oil was treated with 30/40 petroleum ether which precipitated the catalyst which could be reused. Filtration/evaporation yielded the crude product as an oil (77 g). Distillation in vacuo removed 13.1 g hexyl bromide. The yield of undistilled material was 59.3 g (62% based on hexyl bromide).
References:
Lever Brothers Company US4434091, 1984, A
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108-31-6
838 suppliers
$13.47/50 G
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$6.00/100g
![Dioctyl maleate](/CAS/GIF/2915-53-9.gif)
2915-53-9
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$9.00/25g
![CIS-BUTENEDIOIC ANHYDRIDE](/CAS/20180808/GIF/108-31-6.gif)
108-31-6
838 suppliers
$13.47/50 G
![1-Octanol](/CAS/GIF/111-87-5.gif)
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$6.00/100g
![MALEIC ACID MONO(2-ETHYLHEXYL) ESTER](/CAS/GIF/2370-71-0.gif)
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$34.00/25mL
![Dioctyl maleate](/CAS/GIF/2915-53-9.gif)
2915-53-9
176 suppliers
$9.00/25g
![CIS-BUTENEDIOIC ANHYDRIDE](/CAS/20180808/GIF/108-31-6.gif)
108-31-6
838 suppliers
$13.47/50 G
![1-Octanol](/CAS/GIF/111-87-5.gif)
111-87-5
727 suppliers
$6.00/100g
![Dioctyl maleate](/CAS/GIF/2915-53-9.gif)
2915-53-9
176 suppliers
$9.00/25g
![Dioctyl fumarate](/CAS/GIF/2997-85-5.gif)
2997-85-5
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$201.00/250mg