Iron-catalyzed selective production of methyl esters from aldehydes
US-10590062-B1 · Mar 17, 2020 · US
US11827595B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11827595-B2 |
| Application number | US-201917309384-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 12, 2019 |
| Priority date | Nov 13, 2018 |
| Publication date | Nov 28, 2023 |
| Grant date | Nov 28, 2023 |
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A process for direct esterification of an alkyl aldehyde with an alkyl alcohol to produce an alkyl ester is disclosed. The process comprises reacting an alkyl aldehyde with an alkyl alcohol in the presence of an Au/TiOa catalyst, a base and an enal or oxygen to form an ester and an aldehyde. The process avoids liberation of water and avoids the step of oxidation of the alkyl aldehyde to an alkyl acid.
Opening claim text (preview).
We claim: 1. A process for preparing esters comprising: a) combining an alkyl aldehyde with an alkyl enal to form a first mixture; b) heating said mixture in the presence of an Au/TiO 2 catalyst, an alkyl alcohol and in the presence of a base to form a second mixture comprising an alkyl ester and an aldehyde; and c) recovering said alkyl ester and said aldehyde from said second mixture. 2. The process of claim 1 wherein said alkyl alcohol is methanol. 3. The process of claim 1 wherein said alkyl aldehyde is 2-ethylhexaldehyde. 4. The process of claim 1 wherein said alkyl enal is 2-ethylhexyl enal. 5. A process for preparing 2-ethylhexyl methyl ester comprising: a) combining 2-ethylhexaldehyde with 2-ethylhexenal to form a first mixture; b) heating said first mixture in the presence of an Au/TiO 2 catalyst, methanol and in the presence of a base to form a second mixture comprising methyl-2-ethylhexanoate and 2-ethylhexaldehyde; and c) recovering said methyl-2-ethylhexanoate and said 2-ethylhexaldehyde from said second mixture.
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