ChemicalBook CAS DataBase List METHYL NONANOATE

METHYL NONANOATE synthesis

9synthesis methods

Product Name:METHYL NONANOATE
CAS Number:1731-84-6
Molecular formula:C10H20O2
Molecular Weight:172.26

By heating pelargonic acid with methyl alcohol in the presence of concentrated sulfuric acid and subsequent rectification; or by hydrogenation of 1,5-octadien-carboxylic acid methyl ester using palladium chloride in methanol solution.

111-66-0 Synthesis

111-66-0
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107-31-3
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$16.00/25mL

1731-84-6
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$25.00/250mg

2177-86-8 Synthesis

2177-86-8
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5162-60-7
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816-63-7
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Yield:1731-84-6 92.1 %Chromat.

Reaction Conditions:

with methanesulfonic acid;bis(acetylacetonato)palladium(II);1,2-bis[di(t-butyl)phosphinomethyl]benzene in methanol at 100; under 3825.38 Torr; for 20 h;Autoclave;Inert atmosphere;Overall yield = 98 %Chromat.;Temperature;

Steps:

6
A 100 ml stainless steel autoclave is charged with54.5 mmol of 1 -octene (8.5 ml), Pd(acac)2, 0.038 mol % (6.3 mg), 0.13 mol % of l3uPoX (28.4 mg), 10 ml of methyl formate, 10 ml of methanol and 20 tl of methanesulphonic acid under a protective gas (argon or nitrogen for example). The autoclave is heated to 100° C. to establish a final pressure of 5.1 bar, followed by stirring at that temperature for 20 h. The autoclave is subsequently cooled down to room temperature and the residual pressure is released. A 5 ml quantity of isooctane is added to the reaction solution as an internal standard and the mixture is analysed by gas chromatography. The yield of n-product, i.e. methyl nonanoate, is 92.1%. The yield of branched products (methyl 2-methyloctanoate, methyl 2-ethylheptanoate and methyl 2-propylhexanoate) is altogether 5.9%. The total yield of methyl esters is accordingly 98% with an n:iso ratio of 94:6.

References:

EVONIK INDUSTRIES AG;Franke, Robert;Hess, Dieter;Beller, Matthias;Jackstell, Ralf;Cozzula, Daniela;Fleischer, Ivana;Jennerjahn, Reiko US2014/309435, 2014, A1 Location in patent:Paragraph 0042; 0050; 0060