5440-89-1Relevant academic research and scientific papers
Methods to produce fuels
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Page/Page column 59, (2018/02/28)
The present disclosure generally relates to the catalytic conversion of alcohols into hydrocarbon ketones suitable for use as fuels. More specifically, the present disclosure relates to the catalytic conversion of a mixture of isopropanol-butanol-ethanol (IBE) or acetone-butanol-ethanol (ABE), into ketones suitable for use as fuels. The ABE or IBE mixtures may be obtained from the fermentation of biomass or sugars.
METHODS FOR PRODUCING FUELS, GASOLINE ADDITIVES, AND LUBRICANTS
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Paragraph 0173, (2015/01/06)
The present disclosure generally relates to the production of fuels, gasoline additives, and/or lubricants, and precursors thereof. The compounds used to produce the fuels, gasoline additives, and/or lubricants, and precursors thereof may be derived from biomass. The fuels, gasoline additives, and/or lubricants, and precursors thereof may be produced by a combination of intermolecular and/or intramolecular aldol condensation reactions, Guerbet reactions, hydrogenation reactions, and/or oligomerization reactions.
PRO-FRAGRANCE COMPOUNDS
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Page/Page column 21, (2014/12/09)
A compound of Formula (I) wherein R1 represents a C3 to C20 hydrocarbon group derived from a fragrant alcohol of formula R1OH or from a fragrant aryl aldehyde or ketone of Formula (II), wherein: R2 is, independently, hydrogen atom, hydroxyl group, acetoxy group, -O(C=O)CH(CH3), optionally substituted C1-C6 alkyl group or C1-C6 alkoxy group, wherein any two of R2 may form an optionally substituted 5 or 6 membered ring, and R1 represents a radical derived from a fragrant alcohol of formula R1OH or from a fragrant aldehyde or from a fragrant aryl aldehyde or ketone of formula (II). The compounds are useful for example as a precursor for the prolonged delivery or release of fragrant compounds such as fragrant alcohols or aldehydes.
5,13-DIETHYL-10-METHYL-8-HEPTADECANONE: A COMPONENT OF POST-1976 KELEX 100
Striegel, Hans-Guenter,Wiegrebe, Wolfgang
, p. 2203 - 2208 (2007/10/02)
The title compound was prepared by mixed aldol condensation of 2-ethylhexanal and acetone, double bond hydrogenation, aldol autocondenstaion of the resulting saturated ketone and final double bond hydrogenation.It is identical with the ketone C22H44O previously isolated from new Kelex 100 which was erroneoulsy assigned a furoquinoline structure.
